Prosecution Insights
Last updated: April 19, 2026
Application No. 18/143,864

Semi-Automated Ophthalmic Photocoagulation Method and Apparatus

Non-Final OA §DP
Filed
May 05, 2023
Examiner
MOSS, JAMES R
Art Unit
3792
Tech Center
3700 — Mechanical Engineering & Manufacturing
Assignee
Iridex Corporation
OA Round
1 (Non-Final)
51%
Grant Probability
Moderate
1-2
OA Rounds
3y 3m
To Grant
92%
With Interview

Examiner Intelligence

Grants 51% of resolved cases
51%
Career Allow Rate
134 granted / 261 resolved
-18.7% vs TC avg
Strong +41% interview lift
Without
With
+41.0%
Interview Lift
resolved cases with interview
Typical timeline
3y 3m
Avg Prosecution
33 currently pending
Career history
294
Total Applications
across all art units

Statute-Specific Performance

§101
13.3%
-26.7% vs TC avg
§103
36.7%
-3.3% vs TC avg
§102
13.5%
-26.5% vs TC avg
§112
29.5%
-10.5% vs TC avg
Black line = Tech Center average estimate • Based on career data from 261 resolved cases

Office Action

§DP
DETAILED ACTION Notice of Pre-AIA or AIA Status The present application, filed on or after March 16, 2013, is being examined under the first inventor to file provisions of the AIA . Double Patenting The nonstatutory double patenting rejection is based on a judicially created doctrine grounded in public policy (a policy reflected in the statute) so as to prevent the unjustified or improper timewise extension of the “right to exclude” granted by a patent and to prevent possible harassment by multiple assignees. A nonstatutory double patenting rejection is appropriate where the conflicting claims are not identical, but at least one examined application claim is not patentably distinct from the reference claim(s) because the examined application claim is either anticipated by, or would have been obvious over, the reference claim(s). See, e.g., In re Berg, 140 F.3d 1428, 46 USPQ2d 1226 (Fed. Cir. 1998); In re Goodman, 11 F.3d 1046, 29 USPQ2d 2010 (Fed. Cir. 1993); In re Longi, 759 F.2d 887, 225 USPQ 645 (Fed. Cir. 1985); In re Van Ornum, 686 F.2d 937, 214 USPQ 761 (CCPA 1982); In re Vogel, 422 F.2d 438, 164 USPQ 619 (CCPA 1970); In re Thorington, 418 F.2d 528, 163 USPQ 644 (CCPA 1969). A timely filed terminal disclaimer in compliance with 37 CFR 1.321(c) or 1.321(d) may be used to overcome an actual or provisional rejection based on nonstatutory double patenting provided the reference application or patent either is shown to be commonly owned with the examined application, or claims an invention made as a result of activities undertaken within the scope of a joint research agreement. See MPEP § 717.02 for applications subject to examination under the first inventor to file provisions of the AIA as explained in MPEP § 2159. See MPEP § 2146 et seq. for applications not subject to examination under the first inventor to file provisions of the AIA . A terminal disclaimer must be signed in compliance with 37 CFR 1.321(b). The filing of a terminal disclaimer by itself is not a complete reply to a nonstatutory double patenting (NSDP) rejection. A complete reply requires that the terminal disclaimer be accompanied by a reply requesting reconsideration of the prior Office action. Even where the NSDP rejection is provisional the reply must be complete. See MPEP § 804, subsection I.B.1. For a reply to a non-final Office action, see 37 CFR 1.111(a). For a reply to final Office action, see 37 CFR 1.113(c). A request for reconsideration while not provided for in 37 CFR 1.113(c) may be filed after final for consideration. See MPEP §§ 706.07(e) and 714.13. The USPTO Internet website contains terminal disclaimer forms which may be used. Please visit www.uspto.gov/patent/patents-forms. The actual filing date of the application in which the form is filed determines what form (e.g., PTO/SB/25, PTO/SB/26, PTO/AIA /25, or PTO/AIA /26) should be used. A web-based eTerminal Disclaimer may be filled out completely online using web-screens. An eTerminal Disclaimer that meets all requirements is auto-processed and approved immediately upon submission. For more information about eTerminal Disclaimers, refer to www.uspto.gov/patents/apply/applying-online/eterminal-disclaimer. Claims 2, 4-7, 10, 12-15, 18-21 are rejected on the ground of nonstatutory double patenting as being unpatentable over claim 1-5 of U.S. Patent No. 10034796. Although the claims at issue are not identical, they are not patentably distinct from each other because Claim 1 of ‘796 discloses the elements of claims 2, 10, 18: system performing the method for capturing an image of the patient's eye (‘796 Claim 1); locating an area of the patient's eye that indicates a previous treatment (‘796 Claim 1); building a treatment pattern included in a treatment template that identifies the target tissue in a pretreatment image of the patient's eye, wherein the target tissue is not part of the located area (‘796 Claim 1); registering the pretreatment image and the treatment template to the captured image (‘796 Claim 1); setting a position onto which treatment light is to be projected in the patient's eye by using the treatment template (‘796 Claim 1); controlling a delivery system based on the set position so that the treatment light is projected onto the position (‘796 Claim 1); and controlling a dosage of the treatment light at the set position based on a dosage control information (‘796 Claim 1). The remaining recited rejected dependent claims of the current claim set are disclosed by Claims 2-5 of ‘796. Claims 2-21 are rejected on the ground of nonstatutory double patenting as being unpatentable over claim 1-23 of U.S. Patent No. 10398599. ‘599 Claim 13 discloses the current applicants claims 2/10/18. System including deliver, image capture etc. (‘599 Claim 1); capturing an image of a patient's eye via the camera (‘599 Claim 1); locating an area of the patient's eye that indicates a previous treatment (‘599 Claim 13); building a treatment pattern included in a treatment template that identifies target tissue in a pretreatment image of the patient's eye (‘599 Claim 12), wherein the target tissue is not part of the located area (‘599 Claim 13); registering the pretreatment image and the treatment template to the captured image (‘599 Claim 1); setting a position onto which the treatment light is to be projected in the patient's eye by using the treatment template (‘599 Claim 1); controlling the treatment light delivery system based on the set position so that the treatment light is projected onto the position (‘599 Claim 1); and controlling a dosage of the treatment light at the set position based on a dosage control information (‘599 Claim 1). The remaining claims are obvious in view of the remaining claims of ‘599. Claims 2-21 are rejected on the ground of nonstatutory double patenting as being unpatentable over claim 1-18 of U.S. Patent No. 10925768 in view of US 20050288745 to Andersen et al. (included in 8/25/23 IDS). The ‘768 Claim 10 discloses the current applicants claims 2/10/18. Capturing an image of a patient's eye via the camera (‘768 Claim 1); locating an area of the patient's eye that indicates a previous treatment (‘768 Claim 10); building a treatment pattern included in a treatment template that identifies target tissue in a pretreatment image of the patient's eye (‘768 Claim 9), wherein the target tissue is not part of the located area (‘768 Claim 10); registering the pretreatment image and the treatment template to the captured image (‘768 Claim 1); controlling the treatment light delivery system based on the set position so that the treatment light is projected onto the position (‘768 Claim 1). an interpretation of the claims of ‘768 may not explicitly disclose setting a position onto which the treatment light is to be projected in the patient's eye by using the treatment template; and controlling a dosage of the treatment light at the set position based on a dosage control information. However, in the same field of endeavor (medical treatment system), Andersen teaches setting a position onto which the treatment light is to be projected in the patient's eye by using the treatment template ([0040]-[0042], [0045]-[0046], Fig. 6, 9; “sets” the scanning and other optical element into position to apply light); and controlling a dosage of the treatment light at the set position based on a dosage control information ([0032], [0034], [0037]-[0039], [0047], claim 48). It would have been prima facie obvious to one of skill in the art before the effective filing date of the claimed invention to have modified the planning and registration for treatment of ‘768 to include the “setting” and “controlling a dosage . . .” as disclosed by Andersen because the approach provided by Andersen providing a treatment which is overcomes the tedious and time consuming aspects of previous approaches ([0005], [0012]) The remaining claims are obvious in view of the remaining claims of ‘768. Claims 2-21 are rejected on the ground of nonstatutory double patenting as being unpatentable over claim 1-19 of U.S. Patent No. 11672704 in view of US 20050288745 to Andersen et al. ‘704 Claim 10 discloses the current applicants claims 2/10/18. Capturing an image of a patient's eye via the camera (‘704 Claim 1); locating an area of the patient's eye that indicates a previous treatment (‘704 Claim 10); building a treatment pattern included in a treatment template that identifies target tissue in a pretreatment image of the patient's eye (‘704 Claim 9), wherein the target tissue is not part of the located area (‘704 Claim 10); registering the pretreatment image and the treatment template to the captured image (‘704 Claim 1); controlling the treatment light delivery system based on the set position so that the treatment light is projected onto the position (‘704 Claim 1). an interpretation of the claims of ‘704 may not explicitly disclose setting a position onto which the treatment light is to be projected in the patient's eye by using the treatment template; and controlling a dosage of the treatment light at the set position based on a dosage control information. However, in the same field of endeavor (medical treatment system), Andersen teaches setting a position onto which the treatment light is to be projected in the patient's eye by using the treatment template ([0040]-[0042], [0045]-[0046], Fig. 6, 9; “sets” the scanning and other optical element into position to apply light); controlling the treatment light delivery system based on the set position so that the treatment light is projected onto the position ([0040]-[0042], [0044], [0047], claim 48); and controlling a dosage of the treatment light at the set position based on a dosage control information ([0032], [0034], [0037]-[0039], [0047], claim 48). It would have been prima facie obvious to one of skill in the art before the effective filing date of the claimed invention to have modified the planning and registration for treatment of ‘704 to include the “setting” and “controlling a dosage . . .” as disclosed by Andersen because the approach provided by Andersen providing a treatment which is overcomes the tedious and time consuming aspects of previous approaches ([0005], [0012]) The remaining claims are obvious in view of the remaining claims of ‘704. Conclusion The prior art made of record and not relied upon is considered pertinent to applicant's disclosure. US 20040143244 to Gray discuses registration image mapping and briefly treatment patterns US 6099522 included in 8/25/23 IDS US 20040002694 aligns two images one “reference”/prior with higher resolution. The pattern is based on the combination of images. US 20080015553 – Figs. 2-4, 9-10B, [0123] For example a chromakey and/or a luminance key can be used under operator supervision to inhibit delivery of therapeutic laser energy to some treatment locations of a selected treatment pattern that would fall onto retinal locations that correspond with a retinal image of particular characteristics. For example, a mayor blood vessel, a scar, a pigmented zone, the macular area can all provide pixel characteristics to help processor/controller 10 block delivery of therapeutic laser energy onto these locations. US 6599286 – Fig. 2, Claim 17 US 20070161972 - [0038] According to an exemplary embodiment of the invention, and as known in the art, it can be determined whether an eye has previously had photoablative laser surgery by looking at topographic and pachymetric diagnostic information; for example, by analyzing anterior surface topography and delta-pachymetry measurements, the presence and location of a transition zone in the previously ablated cornea can be determined. The irregularity of an eye for purposes of classification can be determined, for example, by examining the symmetry (dipole) of the corneal topography or decentration. US 20060116668 included in 8/25/23 IDS see [0027]-[0032] Any inquiry concerning this communication or earlier communications from the examiner should be directed to JAMES R MOSS whose telephone number is (571)272-3506. The examiner can normally be reached Monday - Friday (9:30 am - 5:30 pm). Examiner interviews are available via telephone, in-person, and video conferencing using a USPTO supplied web-based collaboration tool. To schedule an interview, applicant is encouraged to use the USPTO Automated Interview Request (AIR) at http://www.uspto.gov/interviewpractice. If attempts to reach the examiner by telephone are unsuccessful, the examiner’s supervisor, James Kish can be reached at (571) 272-5554. The fax phone number for the organization where this application or proceeding is assigned is 571-273-8300. Information regarding the status of published or unpublished applications may be obtained from Patent Center. Unpublished application information in Patent Center is available to registered users. To file and manage patent submissions in Patent Center, visit: https://patentcenter.uspto.gov. Visit https://www.uspto.gov/patents/apply/patent-center for more information about Patent Center and https://www.uspto.gov/patents/docx for information about filing in DOCX format. For additional questions, contact the Electronic Business Center (EBC) at 866-217-9197 (toll-free). If you would like assistance from a USPTO Customer Service Representative, call 800-786-9199 (IN USA OR CANADA) or 571-272-1000. /James Moss/Examiner, Art Unit 3792
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Prosecution Timeline

May 05, 2023
Application Filed
Jan 10, 2026
Non-Final Rejection — §DP (current)

Precedent Cases

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Study what changed to get past this examiner. Based on 5 most recent grants.

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Prosecution Projections

1-2
Expected OA Rounds
51%
Grant Probability
92%
With Interview (+41.0%)
3y 3m
Median Time to Grant
Low
PTA Risk
Based on 261 resolved cases by this examiner. Grant probability derived from career allow rate.

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