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Instrument I-K2767KF01

by Howmedica Osteonics Corp.

Instrument I-K2767KF01 is a Class I device made by Howmedica Osteonics Corp., listed in FDA GUDID since 24 Sep 2018 (UDI-DI 07613327306750), 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 Number07613327306750 UDI-DI Date24 Sep 2018ListedStatusListed 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  • Withdrawn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
Instrument
Generic name
Manual goniometer
Model / Ref / Catalog
I-K2767KF01
Primary DI / UDI-DI
07613327306750
FDA product code
LXH
GMDN term
Manual goniometer
Device class
Class I
Regulation number
888.4540
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization
Size
Lumen/Inner Diameter — 0.3125 Inch

Related devices

Category: Manual goniometer

Similar devices

Other devices filed under FDA product code LXH (ORTHOPEDIC MANUAL SURGICAL INSTRUMENT).

Other devices from Howmedica Osteonics Corp.

See all devices from Howmedica Osteonics Corp. →

Properties

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