FDA applicant

Medical Creative Technologies, Inc.

Colmar, PA3 decisions1996–19970 recalls

FDA records 3 decisions for Medical Creative Technologies, Inc. (Colmar, PA) from 1996 to 1997: 3 510(k) clearances. Most are in product codes GCJ (Laparoscope, General & Plastic Surgery) and OCZ (Endoscopic Grasping/Cutting Instrument…). Its devices cite 1 predicate, 1 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 Medical Creative Technologies, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Medical Creative Technologies, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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

See the 510(k) Report

Medical Creative Technologies, Inc.

Which product codes does it file in?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?