Consulting Wallah › Device Explorer › Wound care & sutures › Polytetrafluoroethylene suture
Device Explorer · FDA GUDID · GMDN 17467

Polytetrafluoroethylene suture

A sterile, single-strand (monofilament), synthetic, non-bioabsorbable thread made of expanded polytetrafluoroethylene (ePTFE) intended to join (approximate) the edges of a soft-tissue wound or incision by stitching or to ligate soft tissues; it may include an

US‑registered devices86in commercial distribution
Companies7labelers on GUDID
Single‑use100%of device records
Sterile100%labelled sterile
Prescription55%Rx‑only share
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Share of device records

Riverpoint Medical, Llc4957%
Benco Dental Supply Co.910%
Henry Schein, Inc.910%
Zimvie Us Corp Llc89%
Golnit Sutures78%
C.P. Medical Corporation33%
Origami Surgical Llc11%

Top labelers

CompanyDevicesShare
Riverpoint Medical, Llc4957%
Benco Dental Supply Co.910%
Henry Schein, Inc.910%
Zimvie Us Corp Llc89%
Golnit Sutures78%
C.P. Medical Corporation33%
Origami Surgical Llc11%

Company = labeler of record on GUDID. 7 companies in total; top 12 shown. Click headers to sort.

Brand names on the register (sample)

Golnit PTFE SutureGolnit PTFE SuturesStitchKitOSSEOGUARD®KLOSUREKlosureMONOTEXPTFECYTOSURGGIBSONC-PTFEMaxima

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

FDA product codes

CodeNameDevices
NBYSuture, Surgical, Nonabsorbable, Expanded, Polytetraflouroet69
NBYSUTURE, SURGICAL, NONABSORBABLE, EXPANDED, POLYTETRAFLOUROET17
NAYSystem,Surgical,Computer Controlled Instrument1
GCJLaparoscope, General & Plastic Surgery1

GMDN & GCC registration

  • GMDN code 17467 · non‑implantable
  • Single‑use 100% · sterile 100% · Rx‑only 55% · 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 (Inch) · 15

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

No closely related category with 50+ devices.

How many polytetrafluoroethylene suture products are registered in the US?

86 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Polytetrafluoroethylene suture", from 7 companies. The largest labeler is Riverpoint Medical, Llc with 57% of records.

Which FDA product codes apply?

NBY (Suture, Surgical, Nonabsorbable, Expanded, Polytetraflouroet), NBY (SUTURE, SURGICAL, NONABSORBABLE, EXPANDED, POLYTETRAFLOUROET), NAY (System,Surgical,Computer Controlled Instrument), GCJ (Laparoscope, General & Plastic Surgery)

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.

How do I get quotes?

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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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