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T2 Alpha 2352-3536S

by Stryker Corp.

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

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number07613327566055 UDI-DI Date1 Mar 2024ListedStatusListed 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  • Withdrawn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
T2 Alpha
Generic name
Fluted surgical drill bit, single-use
Model / Ref / Catalog
2352-3536S
Primary DI / UDI-DI
07613327566055
FDA product code
LXH, HWE
GMDN term
Fluted surgical drill bit, single-use
Device class
Class I
Regulation number
888.4540, 878.4820
GUDID distribution status
In Commercial Distribution
Size
Length — 360.0 Millimeter

Related devices

Category: Fluted surgical drill bit, single-use

Other devices from Stryker Corp.

See all devices from Stryker Corp. →

Properties

  • Supplied sterile
  • Single use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Expiration date

Other properties (9)

  • Sterilise before use: No
  • Implantable: No
  • Contains latex: No
  • Over-the-counter: No
  • Convenience kit: No
  • Combination product: No
  • HCT/P: No
  • Serial number: No
  • Manufacturing date: No