510(k) Report

FDA applicant

Slater Endoscopy, LLC

Miami Lakes, FL3 decisions2014–20180 recalls

FDA records 3 decisions for Slater Endoscopy, LLC (Miami Lakes, FL) from 2014 to 2018: 3 510(k) clearances. Most are in product codes OCZ (Endoscopic Grasping/Cutting Instrument…) and KGE (Forceps, Biopsy, Electric). Its devices cite 5 predicates, 2 of them its own earlier devices. No recall is 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 Slater Endoscopy, LLC’s devices, and how often a recall has named them.

FDA decisions per year

1in 2018

2014: 12015: 12018: 1
2014high 1 (2014) · low 0 (2016)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2014.

FIG. 1 — Slater Endoscopy, LLC by year, 2014–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Which product codes does it file in?

  • OCZEndoscopic Grasping/Cutting Instrument, Non-Powered2decisions
  • KGEForceps, Biopsy, Electric1decision

Whose devices does it build on?

Its devices cite 5 predicates; 2 are its own earlier devices. The firms it cites most:

Who builds on its devices?

Later devices cite its devices 3 times; 2 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.

  • K150939Ensizor Endoscopic ScissorsSlater Endoscopy, LLC · 20152cite it
  • K141058Ensizor Endoscopic ScissorsSlater Endoscopy, LLC · 20141cites it

What has FDA decided for it lately?

  • K180134Ensizor Monopolar Endoscopic ScissorsSlater Endoscopy, LLC · 2018
  • K150939Ensizor Endoscopic ScissorsSlater Endoscopy, LLC · 2015
  • K141058Ensizor Endoscopic ScissorsSlater Endoscopy, LLC · 2014

All 3 as Slater Endoscopy, LLC →