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U44-640-16S

by Synthes

U44-640-16S (U4464016S) is a Class I device made by Synthes, listed in FDA GUDID since 18 Jan 2019 (UDI-DI 20705034711079), 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 Number20705034711079 UDI-DI Date18 Jan 2019ListedStatusListed 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  • Withdrawn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

Generic name
Orthopaedic bone pin, non-bioabsorbable
Model / Ref / Catalog
U44-640-16S, U4464016S
Primary DI / UDI-DI
20705034711079
FDA product code
LXH
GMDN term
Orthopaedic bone pin, non-bioabsorbable
Device class
Class I
Regulation number
888.4540
GUDID distribution status
In Commercial Distribution

Related devices

Category: Bone distraction forceps

Similar devices in this category

Other devices filed under Bone distraction forceps.

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Properties

  • Supplied sterile
  • Single use
  • Implantable
  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Expiration date
Other properties (8, all answered No)