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Sonoma Orthopedic Products, Inc. Fib First Gen Bottom Insert Tray

by Arthrex, Inc. GUDID

Listed FDA GUDID listing, not in commercial distribution

Regulatory status

as of 29 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00816988012368 UDI-DIDate7 Jul 2017ListedStatusListed GUDID: not in commercial distribution

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Recalls

0 recalls · FDA

No FDA recalls on record, checked 22 Oct 2026.

Specification

GUDID

Trade Name
Sonoma Orthopedic Products, Inc.
Generic Name
Device sterilization/disinfection container, reusable
Model / Ref / Catalog
Fib First Gen Bottom Insert Tray, IN6803
Primary DI / UDI-DI
00816988012368
FDA Product Code
LXH
GMDN Term
Device sterilization/disinfection container, reusable
Device Class
Class I
Regulation Number
888.4540
GUDID distribution status
Not in Commercial Distribution
Sterilization Method
Moist Heat or Steam Sterilization

Other devices from Arthrex, Inc.

See all devices from Arthrex, Inc. →

Properties

  • Prescription Use
  • Premarket Exempt
  • Lot / Batch Number

Other properties (11)

  • Sterile: No
  • Single Use: No
  • Implantable: No
  • Contains Latex: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Serial Number: No
  • Expiration Date: No
  • Manufacturing Date: No