Vanish™ Varnish

3M™ ESPE™ Vanish™ Varnish, Cherry, 50 Pack, 12159C

Registry build 21.09.26
1manufacturer
3catalogue numbers in this listing
2510(k) clearances naming this product code
1recall

Who Else Makes It

Registered in Hebei.

Chinese manufacturers registered for FDA product code LBH
Manufacturer City Province Registered as Device types
CAO (China) Medical Equipment Company, Limited Langfang Hebei Contract manufacturer 6

Record

Regulatory record for Vanish™ Varnish
Listed by 3M Company, United States
FDA product code LBH
Device type Varnish, Cavity
Device class Class 2
Regulation 21 CFR 872.3260
Establishment Contract manufacturer, Specification developer, Repacker / relabeller, Complaint-file establishment, Manufacturer
Record published 2017-05-11
Record revised 2018-03-29 (version 2)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Single use Yes
Prescription Prescription only
Label carries lot or batch number, expiry date
Packaging Box of 6

Catalogue Numbers

Catalogue numbers for Vanish™ Varnish
Catalogue number Size Per pack Status
12159C 50 In distribution
12159M 50 In distribution
12159L 50 In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
NovaBright Nanova BIO Materials Inc 46
Enamelast Ultradent Products Inc. 41
Nupro® Dentsply Professional 34
Fluorodose Centrix, Inc. 26
VarnishAmerica Medical Products Laboratories, Inc. 24
Voco Profluorid Varnish Voco Gmbh 23
Profisil Kettenbach Gmbh & Co KG 23
Starbright Nanova BIO Materials Inc 22
Wonderful Dental Roses and Rubies, LLC 19
Henry Schein Henry Schein, Inc. 19
Waterpik Ultra Thin & Clear Varnish Water PIK, Inc. 18
Premier Premier Dental Products Co. 17

Showing 12 of 282. All products under Varnish, Cavity

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K151302 2015-09-18
K090519 2009-04-15

Recalls

1 of these is Class II. Class II means a temporary or reversible health consequence. Volume alone is not a quality signal: a manufacturer that ships more recalls more.

Recalls referencing this product code
Initiated FDA class Root cause Reason Quantity Closed
2018-07-06 Class II Mixed-up of materials/components Product has an unpleasant flavor due to a manufacturing process error resulting in an extraneous material being introduced into the product. 73 units (200 pack) 2019-02-26

Source: U.S. FDA establishment registration and device listing records, public domain. Restructured for clarity and searchability. Not affiliated with or endorsed by the FDA. Records are records: nothing here is an offer of sale.

Where China Actually Supplies

Every device page names the company that lists it and the factories registered to make the same thing. These are the sections with the most of them.

5,100manufacturers registered in China
2,581device types they are registered for
340,248device records, each naming its maker
31provinces with a registered manufacturer