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Stem Trial 2015.11.120

by Total Joint Orthopedics, Inc.

Stem Trial 2015.11.120 is a Class I device made by Total Joint Orthopedics, Inc., listed in FDA GUDID since 24 May 2023 (UDI-DI 00810094690717), registry data as of 22 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 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00810094690717 UDI-DI Date24 May 2023ListedStatusListed 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  • Withdrawn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
Stem Trial
Generic name
Knee stem prosthesis trial
Model / reference
2015.11.120
Primary DI / UDI-DI
00810094690717
FDA product code
LXH
GMDN term
Knee stem prosthesis trial
Device class
Class I
Regulation number
888.4540
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Knee stem prosthesis trial

Similar devices

Other devices filed under FDA product code LXH (Orthopedic manual surgical instrument).

Other devices from Total Joint Orthopedics, Inc.

See all devices from Total Joint Orthopedics, Inc. →

Properties

  • Sterilise before use
  • Prescription use
Other properties (13, all answered No)