Skip to content

Recon T-Plate Trials, 1.5mm FIS 720

by Flower Orthopedics Corporation

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

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 Number00840118101226 UDI-DI Date2 May 2018ListedStatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade Name
Recon T-Plate Trials, 1.5mm
Generic Name
Surgical instrument/implant depth limiter, reusable
Model / Reference
FIS 720
Primary DI / UDI-DI
00840118101226
FDA Product Code
HWT
GMDN Term
Surgical instrument/implant depth limiter, reusable
Device Class
Class I
Regulation Number
888.4800
GUDID distribution status
In Commercial Distribution

Related devices

Category: Surgical instrument/implant depth limiter, reusable

Other devices from Flower Orthopedics Corporation

See all devices from Flower Orthopedics Corporation →

Properties

  • Sterile
  • Single Use
  • Prescription Use
  • Premarket Exempt
  • Lot / Batch Number
  • Expiration Date

Other properties (8)

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