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Bencox HA.091.0050

by Corentec Co., Ltd

Bencox HA.091.0050 is a Class I device made by Corentec Co., Ltd, listed in FDA GUDID since 2 Apr 2026 (UDI-DI 08800017270388), 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 Number08800017270388 UDI-DI Date2 Apr 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  • Withdrawn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
Bencox
Generic name
Acetabular orthopaedic reamer
Model / reference
HA.091.0050
Primary DI / UDI-DI
08800017270388
FDA product code
HTO
GMDN term
Acetabular orthopaedic reamer
Device class
Class I
Regulation number
888.4540
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Similar devices

Other devices filed under FDA product code HTO (Reamer).

Other devices from Corentec Co., Ltd

See all devices from Corentec Co., Ltd →

Properties

  • Sterilise before use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Manufacturing date
Other properties (10, all answered No)