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HS Fiber HS264

by Riverpoint Medical LLC

HS Fiber HS264 is a Class II device made by Riverpoint Medical LLC, listed in FDA GUDID since 10 Feb 2022 (UDI-DI 00840277400215), 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

Unverified

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00840277400215 UDI-DI Date10 Feb 2022ListedStatusListed GUDID: in commercial distribution

Official records

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name
HS Fiber
Generic name
Polyolefin/fluoropolymer suture, multifilament
Model / reference
HS264
Primary DI / UDI-DI
00840277400215
FDA product code
GAT
GMDN term
Polyolefin/fluoropolymer suture, multifilament
Device class
Class II
Regulation number
878.5000
GUDID distribution status
In Commercial Distribution

Related devices

Category: Polyolefin/fluoropolymer suture, multifilament

Similar devices in this category

Other devices filed under Polyolefin/fluoropolymer suture, multifilament.

Other devices from Riverpoint Medical LLC

See all devices from Riverpoint Medical LLC →

Properties

  • Supplied sterile
  • Single use
  • Implantable
  • Lot / batch number
  • Expiration date
  • Manufacturing date
Other properties (9, all answered No)