DePuy Synthes 05.003.535S

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

Registry data, not yet checked by deviCERTS. Source GUDID, synced 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

Region	Authorization	Number	Date	Status
United States	GUDID listing	NumberB504OM05003535S0 UDI-DI	Date8 Apr 2021Listed	StatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade Name: DePuy Synthes
Generic Name: Surgical saw blade, reciprocating, reprocessed
Model / Reference: 05.003.535S

Primary DI / UDI-DI: B504OM05003535S0
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

See all devices from Provision →

Properties

Sterile
Single Use
Prescription Use
Premarket Exempt
Lot / Batch Number
Expiration Date
Manufacturing Date

Other properties (7)

Implantable: No
Contains Latex: No
Over-the-Counter: No
Convenience Kit: No
Combination Product: No
HCT/P: No
Serial Number: No