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Zimmer 20090119XC1

by Provision

Zimmer 20090119XC1 is a Class I device made by Provision, listed in FDA GUDID since 25 Nov 2025 (UDI-DI B504OM20090119XC10), 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 NumberB504OM20090119XC10 UDI-DI Date25 Nov 2025ListedStatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade name
Zimmer
Generic name
Surgical saw blade, reciprocating, reprocessed
Model / reference
20090119XC1
Primary DI / UDI-DI
B504OM20090119XC10
FDA product code
GFA
GMDN term
Surgical saw blade, reciprocating, reprocessed
Device class
Class I
Regulation number
878.4820
GUDID distribution status
In Commercial Distribution

Other devices from Provision

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Properties

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