Skip to content

VarnishAmerica 00013

by Medical Products Laboratories, Inc.

Listed FDA GUDID listing, not in commercial distribution

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 Number10310733000138 UDI-DI Date13 Sep 2016ListedStatusListed GUDID: not 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  • Withdrawn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
VarnishAmerica
Generic Name
Dental coating, tooth-desensitizing, professional
Model / Reference
00013
Primary DI / UDI-DI
10310733000138
FDA Product Code
LBH
GMDN Term
Dental coating, tooth-desensitizing, professional
Device Class
Class II
Regulation Number
872.3260
GUDID distribution status
Not in Commercial Distribution

Other devices from Medical Products Laboratories, Inc.

Properties

  • Single Use
  • Lot / Batch Number
  • Expiration Date
  • Manufacturing Date

Other properties (10)

  • Sterile: No
  • Implantable: No
  • Contains Latex: No
  • Prescription Use: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Serial Number: No