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Henry Schein 5700463

by Henry Schein, Inc.

Henry Schein 5700463 is a Class II device made by Henry Schein, Inc., listed in FDA GUDID since 10 Jan 2017 (UDI-DI 00304040039588), 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 Number00304040039588 UDI-DI Date10 Jan 2017ListedStatusListed 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  • Withdrawn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
Henry Schein
Generic name
Poliglecaprone suture
Model / Ref / Catalog
5700463
Primary DI / UDI-DI
00304040039588
FDA product code
GAM
GMDN term
Poliglecaprone suture
Device class
Class II
Regulation number
878.4493
GUDID distribution status
In Commercial Distribution

Related devices

Category: Poliglecaprone suture

Similar devices

Other devices filed under FDA product code GAM (SUTURE, ABSORBABLE, SYNTHETIC, POLYGLYCOLIC ACID).

Other devices from Henry Schein, Inc.

See all devices from Henry Schein, Inc. →

Properties

  • Supplied sterile
  • Single use
  • Prescription use
  • Lot / batch number
  • Expiration date
Other properties (10, all answered No)