Force Fiber IPN000966

by Teleflex Incorporated 2 variants

Force Fiber IPN000966 (SMS101301S) is a Class II device made by Teleflex Incorporated, listed in FDA GUDID since 16 Oct 2015 (UDI-DI 04026704608614), registry data as of 23 Oct 2026.

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None

No authorization documents

Trust

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

Region	Authorization	Number	Date	Status
United States	GUDID listing	Number04026704608614 UDI-DI	Date16 Oct 2015Listed	StatusListed GUDID: in commercial distribution

Official records

AccessGUDID record UDI-DI 04026704608614

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name: Force Fiber
Generic name: Polyolefin/fluoropolymer suture, multifilament
Model / Ref / Catalog: IPN000966, SMS101301S

Primary DI / UDI-DI: 04026704608614
FDA product code: GAT
GMDN term: Polyolefin/fluoropolymer suture, multifilament

Device class: Class II
Regulation number: 878.5000
GUDID distribution status: In Commercial Distribution

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Other devices filed under Polyolefin/fluoropolymer suture, multifilament.

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Properties

Supplied sterile
Single use
Implantable
Prescription use
Lot / batch number
Manufacturing date

Other properties (9, all answered No)