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Tls 5.0 100-05-0204

by Camber Spine Technologies

Tls 5.0 100-05-0204 is a Class I device made by Camber Spine Technologies, listed in FDA GUDID since 1 Nov 2023 (UDI-DI B0301000502040), 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 NumberB0301000502040 UDI-DI Date1 Nov 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  • Withdrawn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
Tls 5.0
Generic name
Bone curette, reusable
Model / reference
100-05-0204
Primary DI / UDI-DI
B0301000502040
FDA product code
LXH
GMDN term
Bone curette, reusable
Device class
Class I
Regulation number
888.4540
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Bone curette, reusable

Other devices from Camber Spine Technologies

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Properties

  • Sterilise before use
  • Prescription use
  • Premarket exempt
Other properties (12, all answered No)