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Tornier Perform IFX730

by Tornier, Inc.

Tornier Perform IFX730 is a reaming power tool attachment (FDA Class I; FDA product code LXH, Orthopedic manual surgical instrument) made by Tornier, Inc., listed in FDA GUDID since 21 Dec 2022 (UDI-DI 00846832086856), 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 Number00846832086856 UDI-DI Date21 Dec 2022ListedStatusListed 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  • Withdrawn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
Tornier Perform
Generic name
Reaming power tool attachment
Model / Ref / Catalog
IFX730
Primary DI / UDI-DI
00846832086856
FDA product code
LXH
GMDN term
Reaming power tool attachment
Device class
Class I
Regulation number
888.4540
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Reaming power tool attachment

Similar devices

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

Other devices from Tornier, Inc.

See all devices from Tornier, Inc. →

Properties

  • Sterilise before use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Expiration date
  • Manufacturing date
Other properties (9, all answered No)