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United Hip System, UTF Stem, Ti Plasma Spray, High Offset 1106-1216

by United Orthopedic Corp.

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

None ongoing

1 closed

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 Number04712771495720 UDI-DI Date24 Oct 2015ListedStatusListed GUDID: in commercial distribution

Recalls

1 recall · FDA

    • Terminated Z-1385-2013 FDA Class II initiated 20 Feb 2013

    The recall of the Loaner Bin and Sterilization Trays for implants and instruments was initiated by Orthopedic Alliance because the directions for use and surgical techniques were not being provided to every physician and for every surgery.

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade Name
United Hip System, UTF Stem, Ti Plasma Spray, High Offset
Generic Name
Coated hip femur prosthesis, modular
Model / Ref / Catalog
1106-1216
Description
UTF stem, Ti plasma spray, high offset, #16.5
Primary DI / UDI-DI
04712771495720
510(k) Number
FDA Product Code
LPH, LZO, KWY
GMDN Term
Coated hip femur prosthesis, modular
Device Class
Class II
Regulation Number
888.3358, 888.3353, 888.3390
GUDID distribution status
In Commercial Distribution

Other devices from United Orthopedic Corp.

See all devices from United Orthopedic Corp. →

Properties

  • Sterile
  • Single Use
  • Implantable
  • Prescription Use
  • Lot / Batch Number
  • Expiration Date

Other properties (8)

  • Contains Latex: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Serial Number: No
  • Manufacturing Date: No