NeoMTA Plus

10 catalogue numbers from MN250, listed by Avalon Biomed, Inc., United States, under Resin, Root Canal Filling. 4 manufacturers in China are registered for this product code.

Registry build 21.09.26
4manufacturers in China registered for this device type
10catalogue numbers in this listing
3510(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 NeoMTA Plus
Listed by Avalon Biomed, Inc., United States
FDA product code KIF
Device type Resin, Root Canal Filling
Device class Class 2
Regulation 21 CFR 872.3820
510(k) K140955
Record published 2017-12-19
Record revised 2021-08-19 (version 4)

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
Storage Special storage condition: Moisture will reduce the shelf life of the powder; Special storage condition: Keep bottle tightly closed; Special storage condition: Do not refrigerate; Special storage condition: Store at room temperature
Sizes Weight 0.5 to 7 g
Distribution end date 2026-01-13

Catalogue Numbers

Catalogue numbers for NeoMTA Plus
Catalogue number Size Status
MN250 Weight 2.5 g Withdrawn
MN050 Weight 0.5 g Withdrawn
N250 Weight 2.5 g Withdrawn
N050 Weight 0.5 g Withdrawn
N100 Weight 1.0 g Withdrawn
MN100 Weight 1.0 g Withdrawn
MN200 Weight 2.0 g Withdrawn
N700 Weight 7.0 g Withdrawn
N600 Weight 6.0 g Withdrawn
N200 Weight 2.0 g Withdrawn

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
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
Calplus Prevest Denpro Limited 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
K161239 2016-09-01
K140955 2014-06-11
K122892 2012-12-11

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