Home › Device types › ORQ
Mesh, Surgical, Deployer
FDA product code ORQ · Class 2 · General, Plastic Surgery
0
Registered devices
48
Adverse events
0
Recalls
6
510(k) clearances
Devices with this code
VENTRALIGHT — Davol Inc.BioBrace® RC Delivery System — Conmed CorporationPhasix — Davol Inc.AccuMesh — Covidien LPPhasix — Davol Inc.AccuMesh — Covidien LPBioinductive Implant with Arthroscopic Delivery System - Large — Smith & Nephew, Inc.Phasix — Davol Inc.VENTRALIGHT — Davol Inc.Bioinductive Implant with Arthroscopic Delivery System - Medium — Smith & Nephew, Inc.Bioinductive Implant with Arthroscopic Delivery System - Hybrid — Smith & Nephew, Inc.Rotation Medical Reconstituted Collagen Scaffold - Arthroscopic, Large — Smith & Nephew, Inc.VENTRALIGHT — Davol Inc.VENTRALIGHT — Davol Inc.Bioinductive Implant with Arthroscopic Delivery System - Large — Smith & Nephew, Inc.Rotation Medical Reconstituted Collagen Scaffold - Arthroscopic, Medium — Smith & Nephew, Inc.BioBrace® RC Delivery System — Conmed CorporationVENTRALIGHT — Davol Inc.Phasix — Davol Inc.VENTRALIGHT — Davol Inc.Phasix — Davol Inc.VENTRALIGHT — Davol Inc.AccuMesh — Covidien LPVENTRALIGHT — 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 docsSourced from public U.S. FDA data. Informational only — not medical or regulatory advice. Not affiliated with the FDA.
