MTApex

MTApex Bioceramic Root Canal Sealer

Registry build 21.09.26
4manufacturers in China registered for this device type
1catalogue number
5510(k) clearances naming this product code

Who Else Makes It

Concentrated in Shanghai (1), Guangxi (1), Beijing (1).

Chinese manufacturers registered for FDA product code KIF
Manufacturer City Province Registered as Device types
Shanghai JPY ION-Tech Co., Ltd. Shanghai Shanghai Contract manufacturer 70
Guilin Kevin Peter Technology Co., Ltd. Guilin Guangxi Manufacturer 13
Beijing C-Root Dental Medical Devices Co., Ltd. Beijing Beijing Manufacturer 6
Enpuno Biotechnology Co., Ltd. Changsha Hunan Manufacturer 1

Record

Regulatory record for MTApex
Listed by Ultradent Products Inc., United States
FDA product code KIF
Device type Resin, Root Canal Filling
Device class Class 2
Regulation 21 CFR 872.3820
Establishment Contract manufacturer, Repacker / relabeller, Manufacturer
510(k) K181917
Record published 2021-11-24
Record revised 2021-12-08 (version 2)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Prescription Prescription only
Supplied as a kit Yes
Label carries lot or batch number, expiry date

Catalogue Numbers

Catalogue numbers for MTApex
Catalogue number Size Status
4900 In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Brasseler USA Peter Brasseler Holdings, LLC 19
Root canal repair materials Enpunuo Biotechnology Co., Ltd. 12
Diapaste Diadent Group Intl., Inc. 10
NeoMTA Plus Avalon Biomed, Inc. 10
C-Root Beijing C-Root Dental Medical Devices Co., Ltd. 10
MetaSEAL™ Parkell, Inc. 7
Henry Schein Henry Schein, Inc. 7
Grey MTA Plus Avalon Biomed, Inc. 7
EndoREZ Ultradent Products Inc. 6
Cerafill RCS Prevest Denpro Limited 6
MTA Angelus Angelus Industria DE Produtos Odontologicos S/A 5
Injectable Root Canal Bioceramic Sealer(nRoot SP) Enpunuo Biotechnology Co., Ltd. 5

Showing 12 of 204. All products under Resin, Root Canal Filling

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K211905 2021-10-13
K071106 2007-05-08
K042756 2004-10-26
K992097 1999-10-26
K971899 1997-06-26

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