Skip to content

Lip Hook 973-0313

by Kerr Corporation

Lip Hook 973-0313 is a Class II device made by Kerr Corporation, listed in FDA GUDID since 5 Mar 2021 (UDI-DI 00195062031052), 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 Number00195062031052 UDI-DI Date5 Mar 2021ListedStatusListed 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  • Withdrawn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
Lip Hook
Generic name
Dental pulp analysis system
Model / reference
973-0313
Primary DI / UDI-DI
00195062031052
FDA product code
EAT
GMDN term
Dental pulp analysis system
Device class
Class II
Regulation number
872.1720
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Dental pulp analysis system

Other devices from Kerr Corporation

See all devices from Kerr Corporation →

Properties

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