UltraSeal

Sample U-Seal XT Hydro

Registry build 21.09.26
1manufacturer
2catalogue numbers in this listing
7510(k) clearances naming this product code
1recall

Who Else Makes It

Registered in Shandong.

Chinese manufacturers registered for FDA product code EBC
Manufacturer City Province Registered as Device types
Rizhao Huge Biomaterials Company, Ltd. Rizhao Shandong Manufacturer 7

Record

Regulatory record for UltraSeal
Listed by Ultradent Products Inc., United States
FDA product code EBC
Device type Sealant, Pit And Fissure, And Conditioner
Device class Class 2
Regulation 21 CFR 872.3765
Establishment Contract manufacturer, Repacker / relabeller, Manufacturer
510(k) K112517
Record published 2016-09-22
Record revised 2022-08-16 (version 5)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Single use Yes
Prescription Prescription only
Supplied as a kit Yes
Label carries lot or batch number, expiry date
Storage Storage environment temperature 2 to 27 °C

Catalogue Numbers

Catalogue numbers for UltraSeal
Catalogue number Size Status
S3529 In distribution
S3529 In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
UltraSeal XT Ultradent Products Inc. 22
SciPharm Pit & Fissure Sealer Bonding Agent Scientific Pharmaceuticals, Inc. 20
Orthosource Orthosource, Inc. 20
Visalys Fill Kettenbach Gmbh & Co KG 14
Riva Protect SDI Ltd. 14
Venus Diamond Flow Kulzer SRL 9
Conseal SDI Ltd. 9
Delton® Dentsply Professional 9
Helioseal Clear F F Plus Ivoclar Vivadent Aktiengesellschaft 8
Patterson® Patterson Dental Supply, Inc. 8
Clinpro™ 3M Company 7
Visalys Flow Kettenbach Gmbh & Co KG 7

Showing 12 of 133. All products under Sealant, Pit And Fissure, And Conditioner

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K112517 2011-09-23
K101245 2010-09-17
K993846 2000-02-16
K931868 1993-07-22
K931869 1993-07-22
K921600 1992-09-28
K921599 1992-09-28

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
2016-11-17 Class II Labeling mix-ups There was a labeling error with product, UltraSeal XT Plus Clear Refill, Part Number (PN) 565, Lot Number (Lot) BD79T. The package was mislabeled as PQ1, PN 641; while the barcode, IFU and products were labeled for UltraSeal XT Plus Clear 31 2017-06-05

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