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Stryker 5290-635-000

by Provision

Stryker 5290-635-000 is a Class I device made by Provision, listed in FDA GUDID since 8 Jun 2023 (UDI-DI B504ES52906350000), 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 NumberB504ES52906350000 UDI-DI Date8 Jun 2023ListedStatusListed 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  • Withdrawn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
Stryker
Generic name
ENT shaver system
Model / reference
5290-635-000
Primary DI / UDI-DI
B504ES52906350000
FDA product code
EQJ
GMDN term
ENT shaver system
Device class
Class I
Regulation number
874.4140
GUDID distribution status
In Commercial Distribution

Related devices

Category: ENT shaver system

Similar devices

Also classified as ENT shaver system.

Other devices from Provision

See all devices from Provision →

Properties

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