510(k) Report

FDA applicant

J. Jamner Surgical Instruments, Inc.

Great Neck, NY11 decisions1977–20082 recalls

FDA records 11 decisions for J. Jamner Surgical Instruments, Inc. (Great Neck, NY) from 1977 to 2008: 11 510(k) clearances. Most are in product codes GCJ (Laparoscope, General & Plastic Surgery) and EOB (Nasopharyngoscope (Flexible Or Rigid)). 2 recalls are linked to its devices.

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly, last Nov 3, 2026

FIG. A — Illustration, gastroenterology and urology panel, where it files most

How often FDA has decided J. Jamner Surgical Instruments, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

1in 2008

2008: 1
2007high 1 (2008) · low 0 (2007)2026

2026 so far, outlined.

Recalls per year

1in 2014

2013: 12014: 1
2007high 1 (2013) · low 0 (2007)2026

Class I Class II/III not classified

FIG. 1 — J. Jamner Surgical Instruments, Inc. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like J. Jamner Surgical Instruments, Inc.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

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Which product codes does it file in?

  • GCJLaparoscope, General & Plastic Surgery3decisions
  • EOBNasopharyngoscope (Flexible Or Rigid)2decisions
  • GEIElectrosurgical, Cutting & Coagulation & Accessories2decisions
  • HDCTenaculum, Uterine1decision
  • DWSInstruments, Surgical, Cardiovascular1decision
  • KNFCoagulator-Cutter, Endoscopic, Unipolar (And Accessories)1decision

Also: GEN (1).

Who builds on its devices?

Later devices cite its devices 3 times; 0 of those are its own. The firms that cite it most:

Which of its devices are cited most?

Its devices that later submissions most often claim equivalence to.

  • K932456Jarit Surgical InstrumentsJ. Jamner Surgical Instruments, Inc. · 19942cite it
  • K941565Jarit Recommended Sinus InstrumentsJ. Jamner Surgical Instruments, Inc. · 19941cites it

What has FDA decided for it lately?

  • K082349Jarit Hulka Uterine Tenaculum ForcepsJ. Jamner Surgical Instruments, Inc. · 20081 recall
  • K944670Jarit Recommended Sinus InstrumentsJ. Jamner Surgical Instruments, Inc. · 1995
  • K944870Jarit Endoscopes, Models 600-600; 600-630; 600-650; and 600-680J. Jamner Surgical Instruments, Inc. · 1994
  • K941565Jarit Recommended Sinus InstrumentsJ. Jamner Surgical Instruments, Inc. · 1994
  • K932456Jarit Surgical InstrumentsJ. Jamner Surgical Instruments, Inc. · 19941 recall
  • K933728Jarit Surgical Instruments: Catalog 615-330, 615-331, 615-334, 615-335, 615-338, 615-339J. Jamner Surgical Instruments, Inc. · 1994
  • K931928Jarit Surgical InstrumentsJ. Jamner Surgical Instruments, Inc. · 1993
  • K931959Jarit Surgical InstrumentsJ. Jamner Surgical Instruments, Inc. · 1993

All 11 as J. Jamner Surgical Instruments, Inc. →

What has been recalled?

2 recalls linked to its devices; the latest:

  • K082349FIBERNET Embolic Protection System: Recommended Vessel Diameter 6.0 -7.0 mm, Maximum…Mar 3, 2014Class II
  • K932456Integra (R) Jarit (R) Monopolar Cable (Catalogue No. 600-290). For use in endoscopic…Feb 12, 2013Class II