FDA applicant

Endolap, Inc.

Orlando, FL5 decisions1994–19970 recalls

FDA records 5 decisions for Endolap, Inc. (Orlando, FL) from 1994 to 1997: 5 510(k) clearances. Most are in product codes FAS (Electrode, Electrosurgical, Active, Urological) and HET (Laparoscope, Gynecologic (And Accessories)). 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 Endolap, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Endolap, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Endolap, Inc.

Which product codes does it file in?

What has FDA decided for it lately?