A-Dec

A-dec 351AR Radius Assistant's Instrumentation, Certified Pre-Owned

Registry build 21.09.26
13manufacturers in China registered for this device type
66catalogue numbers in this listing
25510(k) clearances naming this product code

Who Else Makes It

Concentrated in Guangdong (8), Shanghai (2), Jiangsu (1). One is registered as a contract manufacturer, able to build to a specification.

Chinese manufacturers registered for FDA product code EIA
Manufacturer City Province Registered as Device types
Acot Plastics (Xiamen) Co., Ltd. Xiamen Fujian Contract manufacturer 8
Lakong Medical Devices Co., Ltd. Dongguan Guangdong Remanufacturer 39
Guangzhou Ajax Medical Equipment Co Ltd Guangzhou Guangdong Manufacturer 13
Jiangsu Dynamic Medical Technology Co., Ltd. Suzhou Jiangsu Manufacturer 12
FDC Technology Industry Company Taishan,Guang Chong Guangdong Manufacturer 6
Foshan Gladent Medical Instrument Co., Ltd. Foshan Guangdong Manufacturer 6
Sinol Dental Limited Xianyang Shaanxi Manufacturer 5
Shanghai Dental Instrument Factory Co., Ltd. Shanghai Shanghai Manufacturer 3
Guangdong Yadeng Medical Apparatus Co., Ltd. Foshan Guangdong Manufacturer 2
Mipont Medical Equipment Co., Ltd. Guangzhou Guangdong Manufacturer 2
Foshan Safety Medical Equipment Co., Ltd. China Guangdong Manufacturer 1
Shanghai Fimet Medical Instrument Co., Ltd. Shang Hai Shanghai Manufacturer 1

Showing 12 of 13. All 13 manufacturers in China registered for Unit, Operative Dental

Record

Regulatory record for A-dec
Listed by A-dec, Inc., United States
FDA product code EIA
Device type Unit, Operative Dental
Device class Class 1
Regulation 21 CFR 872.6640
Establishment Specification developer, Repacker / relabeller, Complaint-file establishment, Manufacturer
510(k) K213932
Record published 2023-05-10
Record revised 2023-04-20 (version 4)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Sterilisation Moist Heat or Steam Sterilization
Label carries lot or batch number, manufacturing date, serial number
Distribution end date 2023-04-25

Catalogue Numbers

Catalogue numbers for A-dec
Catalogue number Size Status
551sta In distribution
334R In distribution
332flt In distribution
11.0233.00 In distribution
541 In distribution
533pro In distribution
3420 In distribution
335R In distribution
342 In distribution
352R In distribution
334pro In distribution
332 In distribution
533R In distribution
532R In distribution
11.0232.00 In distribution
541pro In distribution
353R In distribution
351R In distribution
7004 In distribution
532R In distribution
353 In distribution
4635 In distribution
333pro In distribution
200DSA In distribution
8500B In distribution
342pro In distribution
335 In distribution
336R In distribution
11.0232.80 In distribution
352 In distribution
332R In distribution
533 In distribution
341flt In distribution
2562 In distribution
2561 In distribution
4631 In distribution
542 In distribution
334 In distribution
336R In distribution
532 In distribution
351R In distribution
341pro In distribution
336pro In distribution
335R In distribution
334R In distribution
333 In distribution
200ASA In distribution
343pro In distribution
2671 In distribution
545sta In distribution
551R In distribution
551 In distribution
341sp In distribution
545 In distribution
332pro In distribution
336 In distribution
345 In distribution
335pro In distribution
333R In distribution
2615 In distribution
351 In distribution
532pro In distribution
533A Withdrawn
8100B Withdrawn
532A Withdrawn
541A Withdrawn

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Stradis Stradis Healthcare 305
Forest Ls Enterprises, Inc. 285
DCI DCI International, LLC 201
DCI Edge DCI International, LLC 149
Aseptico Aseptico, Inc. 29
Midmark Midmark Corporation 27
Unit, Operative Dental Ergonomic Products, Inc. 20
TPS Stryker GmbH 20
Evogue Dental Unit Takara Belmont Corporation 20
Belmont X-Calibur Unit Takara Belmont Corporation 19
Dentacenter Operative Dental Unit Safari Dentaire Inc 12
Unit, Operative Dental Stryker GmbH 11

Showing 12 of 224. All products under Unit, Operative Dental

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K213932 2022-03-02
K102234 2010-11-24
K082985 2008-12-17
K051657 2005-08-30
K032757 2003-12-10
K032756 2003-12-04
K032070 2003-08-27
K000968 2000-05-03
K000966 2000-05-03
K000967 2000-05-03
K962665 1996-08-22
K960506 1996-03-25
K940893 1994-07-12
K935325 1994-04-21
K925798 1994-01-06
K925797 1994-01-06
K933166 1993-10-20
K933167 1993-10-13
K933168 1993-10-12
K933163 1993-10-12
K933165 1993-10-12
K903455 1990-10-24
K903452 1990-10-24
K903453 1990-10-24
K903451 1990-10-24

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