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Bosworth Hydrox 0921072

by Harry J. Bosworth Co.

Bosworth Hydrox 0921072 is a Class II device made by Harry J. Bosworth Co., listed in FDA GUDID since 15 Sep 2016 (UDI-DI H66809210721), 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 NumberH66809210721 UDI-DI Date15 Sep 2016ListedStatusListed 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  • Withdrawn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
Bosworth Hydrox
Generic name
Dental pulp-capping material
Model / Ref / Catalog
0921072
Description
Cavity Liner Base & Catalyst Ivory Kit
Primary DI / UDI-DI
H66809210721
FDA product code
EJK
GMDN term
Dental pulp-capping material
Device class
Class II
Regulation number
872.3250
GUDID distribution status
In Commercial Distribution

Related devices

Category: Dental pulp-capping material

Similar devices

Other devices filed under FDA product code EJK (LINER, CAVITY, CALCIUM HYDROXIDE).

Other devices from Harry J. Bosworth Co.

See all devices from Harry J. Bosworth Co. →

Properties

  • Prescription use
  • Convenience kit
  • Lot / batch number
  • Expiration date
Other properties (11, all answered No)