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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. — BIOSEALPOLY SUTURE BUTTON — Biomet Sports Medicine, LLCBioseal Inc. — BIOSEALXTENDOBUTTON — Smith & Nephew, Inc.Q-Stop — DRS Vascular, Inc.MEDLINE — MEDLINE INDUSTRIES, INC.SUTUREGARD Intraoperative Skin Relaxation Device — SUTUREGARD MEDICAL, INCBioseal Inc. — BIOSEALArthrex® — ARTHREX, INC.ETHICON — ETHICON, LLCMedline — MEDLINE INDUSTRIES, INC.Arthrex® — ARTHREX, INC.XTENDOBUTTON — Smith & Nephew, Inc.Bolsters — Covidien LPNA — Smith & Nephew, Inc.StarGuard Suture Retention Plates - 7" — PRESERVATION SOLUTIONS INCDynamic Tissue Systems™ — Southmedic IncorporatedPerchik Button™ — Merit Medical Systems, Inc.MEDLINE RENEWAL — MEDLINE INDUSTRIES, INC.FlowStasis — Inari Medical, Inc.SUTUREGARD(R) Classic Adhesive Suture Retention Device — SUTUREGARD MEDICAL, INCHEMIGARD Adhesive Suture Retention Device — SUTUREGARD MEDICAL, INCBioseal Inc. — BIOSEALXTENDOBUTTON — Smith & Nephew, 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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