FDA applicant

Medical Polymers, Inc.

Austin, TX3 decisions1992–19940 recalls

FDA records 3 decisions for Medical Polymers, Inc. (Austin, TX) from 1992 to 1994: 3 510(k) clearances. Most are in product codes EFB (Handpiece, Air-Powered, Dental) and KOT (Carboxymethylcellulose Sodium Or Polyvinyl…). 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, dental panel, where it files most

How often FDA has decided Medical Polymers, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Medical Polymers, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Medical Polymers, 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 Polymers, Inc.

Which product codes does it file in?

What has FDA decided for it lately?