Osstell SmartPeg Type 55

Catalogue number Osstell SmartPeg Type 55, listed by Osstell AB, Sweden, under Handpiece, Direct Drive, Ac-Powered. 10 manufacturers in China are registered for this product code.

Registry build 21.09.26
10manufacturers in China registered for this device type
1catalogue number
4510(k) clearances naming this product code

Who Else Makes It

Concentrated in Guangdong (6), Jiangsu (2), Guangxi (1). One is registered as a contract manufacturer, able to build to a specification.

Chinese manufacturers registered for FDA product code EKX
Manufacturer City Province Registered as Device types
Jung Chen Technology Co., Ltd. Zhuhai Guangdong Contract manufacturer 2
Shenzhen Rogin Medical Co., Ltd. Shenzhen Guangdong Contract manufacturer 51
Guilin Woodpecker Medical Instrument Co., Ltd. Guilin Guangxi Manufacturer 25
Foshan Coxo Medical Instrument Co., Ltd. Foshan Guangdong Manufacturer 19
Denjoy Dental Co., Ltd. Changsha Hunan Contract manufacturer 17
Foshan Cicada Dental Instrument Co., Ltd. Foshan Guangdong Manufacturer 15
Changzhou Sifary Medical Technology Co., Ltd. Changzhou Jiangsu Manufacturer 14
Shenzhen Superline Technology Co., Ltd. Shenzhen Guangdong Contract manufacturer 12
Shenzhen Perfect Medical Instruments Co., Ltd. Shenzhen Guangdong Manufacturer 10
Changzhou Bomedent Medical Technology Co., Ltd. Changzhou Jiangsu Contract manufacturer 6

Record

Regulatory record for Osstell SmartPeg Type 55
Listed by Osstell AB, Sweden
FDA product code EKX
Device type Handpiece, Direct Drive, Ac-Powered
Device class Class 1
Regulation 21 CFR 872.4200
Establishment Manufacturer
Record published 2022-09-02
Record revised 2024-09-19 (version 2)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Supplied sterile Yes
Single use Yes
Prescription Prescription only
Label carries lot or batch number, expiry date
Packaging Box of 5

Catalogue Numbers

Catalogue numbers for Osstell SmartPeg Type 55
Catalogue number Size Status
Osstell SmartPeg Type 55 In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
MulTipeg™ Integration Diagnostics Sweden AB 151
Aseptico Aseptico, Inc. 40
Brasseler USA Peter Brasseler Holdings, LLC 26
Woodpecker Guilin Woodpecker Medical Instrument Co., Ltd. 16
DTE Guilin Woodpecker Medical Instrument Co., Ltd. 16
Delfin2 Intra-Lock International 16
Ultrapro TX Cordless Ultradent Products Inc. 13
CanalPro Coltene/Whaledent Gmbh & Co. KG 12
ChecQPEG Dentis Co., Ltd. 12
EdgeApex HP™ US Endodontics, LLC 11
Penguin RFA Integration Diagnostics Sweden AB 10
Henry Schein Henry Schein, Inc. 9

Showing 12 of 307. All products under Handpiece, Direct Drive, Ac-Powered

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K181888 2019-08-22
K142358 2015-02-19
K132401 2014-04-09
K082523 2008-09-26

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