FDA Device Intelligence
Home › Device types › ORQ

Mesh, Surgical, Deployer

FDA product code ORQ · Class 2 · General, Plastic Surgery

34
Registered devices
48
Adverse events
0
Recalls
6
510(k) clearances

Devices with this code

Phasix — Davol Inc.VENTRALIGHT — Davol Inc.Phasix — Davol Inc.Rotation Medical Reconstituted Collagen Scaffold - Arthroscopic, Medium — Smith & Nephew, Inc.Phasix — Davol Inc.Phasix — Davol Inc.VENTRALIGHT — Davol Inc.Phasix — Davol Inc.VENTRALIGHT — Davol Inc.Rotation Medical Reconstituted Collagen Scaffold - Arthroscopic, Large — Smith & Nephew, Inc.VENTRALIGHT — Davol Inc.Bioinductive Implant with Arthroscopic Delivery System - Medium — Smith & Nephew, Inc.VENTRALIGHT — Davol Inc.Phasix — Davol Inc.Phasix — Davol Inc.Rotation Medical Reconstituted Collagen Scaffold - Arthroscopic, Hybrid — Smith & Nephew, Inc.VENTRALIGHT — Davol Inc.VENTRALIGHT — Davol Inc.VENTRALIGHT — Davol Inc.AccuMesh — Covidien LPAccuMesh — Covidien LPVENTRALIGHT — Davol Inc.Phasix — Davol Inc.VENTRALIGHT — Davol Inc.

Query this across every FDA database — by API.

Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

Get your free API keyRead the docs
Sourced from public U.S. FDA data. Informational only — not medical or regulatory advice. Not affiliated with the FDA.