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TaperSet Hip System 1910-3-1135

by Shalby Advanced Technologies, Inc.

TaperSet Hip System 1910-3-1135 is a Class I device made by Shalby Advanced Technologies, Inc., listed in FDA GUDID since 9 Jul 2026 (UDI-DI 00840286859974), 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 Number00840286859974 UDI-DI Date9 Jul 2026ListedStatusListed 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  • Withdrawn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
TaperSet Hip System
Generic name
Femoral stem prosthesis trial
Model / Ref / Catalog
1910-3-1135
Primary DI / UDI-DI
00840286859974
FDA product code
HWT
GMDN term
Femoral stem prosthesis trial
Device class
Class I
Regulation number
888.4800
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Other devices from Shalby Advanced Technologies, Inc.

See all devices from Shalby Advanced Technologies, Inc. →

Properties

  • Sterilise before use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
Other properties (11, all answered No)