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Retention Device, Suture
FDA product code KGS · Class 1 · General, Plastic Surgery
73
Registered devices
251
Adverse events
2
Recalls
20
510(k) clearances
Devices with this code
Bioseal Inc. — BIOSEALSUTUREGARD(R) Hammerhead(TM) Adhesive Suture Retention Device — SUTUREGARD MEDICAL, INCXTENDOBUTTON — Smith & Nephew, Inc.V-Close — DRS Vascular, Inc.POLY SUTURE BUTTON — Biomet Sports Medicine, LLCMedline Industries, Inc. — MEDLINE INDUSTRIES, INC.Dynamic Tissue Systems™ — Southmedic IncorporatedMEDLINE RENEWAL — MEDLINE INDUSTRIES, INC.XTENDOBUTTON — Smith & Nephew, Inc.Bioseal Inc. — BIOSEALXTENDOBUTTON — Smith & Nephew, Inc.StarGuard Suture Retention Plates - 7" — PRESERVATION SOLUTIONS INCBioseal Inc. — BIOSEALHEMIGARD Adhesive Suture Retention Device — SUTUREGARD MEDICAL, INCBioseal Inc. — BIOSEALPerchik — ANGIODYNAMICS, INC.HEWSON LIGAMENT BUTTON — Smith & Nephew, Inc.Arthrex® — ARTHREX, INC.SVELTEFELT™ QUICK PLEDGE™ — LSI Solutions, Inc.Slip-Not® — Merit Medical Systems, Inc.Bioseal Inc. — BIOSEALBolsters — Covidien LPBioseal Inc. — BIOSEALMedline — MEDLINE INDUSTRIES, INC.
Recent recalls
| Date | Firm | Reason |
|---|---|---|
| 2025-05-16 | Drs Vascular, Inc | XXX |
| 2006-03-24 | Smith & Nephew, Inc. Endoscopy Division | The implant consists of a T1 and T2 anchor which are joined together by a suture. The T2 portion of the implant may not advance into the deployment position pre |
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