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Device Explorer · FDA GUDID · GMDN 33519

Suture retention device

A device designed to be placed on the surface of the skin and intended to aid wound healing by distributing suture tension over a larger area in the patient. It is typically in the form of a retention bridge, a surgical button, or a suture bolster through whic

US‑registered devices61in commercial distribution
Companies13labelers on GUDID
Single‑use100%of device records
Sterile97%labelled sterile
Prescription56%Rx‑only share
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Share of device records

Bioseal2033%
Ethicon, Llc1525%
Suturegard Medical, Inc47%
Merit Medical Systems, Inc.35%
Inari Medical, Inc.35%
Preservation Solutions Inc35%
Johnson & Johnson International Inc.35%
Boston Medical Products, Inc.23%

Top labelers

CompanyDevicesShare
Bioseal2033%
Ethicon, Llc1525%
Suturegard Medical, Inc47%
Merit Medical Systems, Inc.35%
Inari Medical, Inc.35%
Preservation Solutions Inc35%
Johnson & Johnson International Inc.35%
Boston Medical Products, Inc.23%
Drs Vascular, Inc.23%
Applied Medical Technology, Inc.23%
Covidien Lp23%
Catheter Precision, Inc.12%

Company = labeler of record on GUDID. 13 companies in total; top 12 shown. Click headers to sort.

Brand names on the register (sample)

Stent ButtonsSlip-Not®V-CloseQ-StopSUTUREGARD(R) Hammerhead(TM) Adhesive Suture RetSUTUREGARD(R) Classic Adhesive Suture Retention SUTUREGARD Intraoperative Skin Relaxation DeviceHEMIGARD Adhesive Suture Retention DeviceLockeT Suture Retention DeviceFlowStasis Single-PackFlowStasisATLAS Suture Delivery System"StarGuard Suture Retention Plates - 9""""StarGuard Suture Retention Plates - 7"""Bioseal Inc.Purstring

Sample of brand names as labelled; no endorsement. Ask us for the full list with company, model and UDI.

FDA product codes

CodeNameDevices
KGSRETENTION DEVICE, SUTURE26
DXZPATCH, PLEDGET AND INTRACARDIAC, PETP, PTFE, POLYPROPYLENE18
KGSRetention Device, Suture15
KGCTube, Gastro-Enterostomy2
GDJCLAMP, SURGICAL, GENERAL & PLASTIC SURGERY2

GMDN & GCC registration

  • GMDN code 33519 · non‑implantable
  • Single‑use 100% · sterile 97% · Rx‑only 56% · OTC 0%
  • UAE: MOHAP / DoH medical device registration and an authorised representative are required; Saudi: SFDA MDMA. We check status on request.

Size attributes recorded

Length (Millimeter) · 2Length (Inch) · 1Height (Inch) · 1Outer Diameter (Inch) · 1

Use these as the dimensions to specify in a tender line.

How many suture retention device products are registered in the US?

61 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Suture retention device", from 13 companies. The largest labeler is Bioseal with 33% of records.

Which FDA product codes apply?

KGS (RETENTION DEVICE, SUTURE), DXZ (PATCH, PLEDGET AND INTRACARDIAC, PETP, PTFE, POLYPROPYLENE), KGS (Retention Device, Suture), KGC (Tube, Gastro-Enterostomy)

Is this the same as UAE/GCC registration?

No. GUDID is the US register. For the UAE (MOHAP/DoH) and Saudi (SFDA/MDMA) a separate registration and a local authorised representative are required; Consulting Wallah can check the status and connect you with registered suppliers.

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Source: FDA AccessGUDID (AccessGUDID full release 2 Nov 2026); counts are device records in commercial distribution grouped by GMDN preferred term; companies are labelers of record. Information only — US listing is not a registration in the UAE or GCC; verify with the regulator. © Consulting Wallah — CC BY‑NC‑ND.

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