Instruments PS PSR PSL

Catalogue number FS-459, listed by E.M.S. Electro Medical Systems S.A., Switzerland, under Scaler, Ultrasonic. 14 manufacturers in China are registered for this product code.

Registry build 21.09.26
14manufacturers in China registered for this device type
1catalogue number
10510(k) clearances naming this product code
3recalls on this code

Who Else Makes It

Concentrated in Guangdong (4), Guangxi (4), Shandong (2). 2 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code ELC
Manufacturer City Province Registered as Device types
Zibo Dante Co., Ltd. Zibo Shandong Contract manufacturer 17
China Zhong YAN Chang Xing International Co., Ltd. Zibo Shandong Contract manufacturer 5
Lakong Medical Devices Co., Ltd. Dongguan Guangdong Remanufacturer 39
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
Wenzhou Baiyu Glasses Technology Co., Ltd. Wenzhou Zhejiang Contract manufacturer 10
Shenzhen Ainengke Electronics Co., Ltd. Shenzhen Guangdong Manufacturer 9
Guilin Refine Medical Instrument Co., Ltd. Guilin Guangxi Contract manufacturer 7
Shenzhen Micro Electric Intelligence Co., Ltd. Shenzhen Guangdong Manufacturer 7
Changzhou Bomedent Medical Technology Co., Ltd. Changzhou Jiangsu Contract manufacturer 6
Nanning Baolai Medical Instrument Co., Ltd. Nanning Guangxi Manufacturer 4

Showing 12 of 14. All 14 manufacturers in China registered for Scaler, Ultrasonic

Record

Regulatory record for Instruments PS PSR PSL
Listed by E.M.S. Electro Medical Systems S.A., Switzerland
FDA product code ELC
Device type Scaler, Ultrasonic
Device class Class 2
Regulation 21 CFR 872.4850
Establishment Remanufacturer, Specification developer, Repacker / relabeller, Complaint-file establishment, Manufacturer, Exporter
510(k) K253254
Record published 2026-02-16

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Sterilisation Moist Heat or Steam Sterilization
Prescription Prescription only
Label carries lot or batch number, manufacturing date
UDI direct marking Exempt

Catalogue Numbers

Catalogue numbers for Instruments PS PSR PSL
Catalogue number Size Status
FS-459 In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Woodpecker Guilin Woodpecker Medical Instrument Co., Ltd. 501
Piezon E.M.S. Electro Medical Systems S.A. 245
Acteon Satelec 236
Mectron Mectron SPA 209
Varios Nakanishi Inc. 158
BioSonic Coltene/Whaledent Gmbh & Co. KG 142
Cavitron® Dentsply Professional 137
DTE Guilin Woodpecker Medical Instrument Co., Ltd. 113
Hu-Friedy HU-Friedy MFG Co., LLC 83
Obtura Spartan Obtura Spartan Endodontics 74
Henry Schein Henry Schein, Inc. 48
Baolai Nanning Baolai Medical Instrument Co., Ltd. 46

Showing 12 of 653. All products under Scaler, Ultrasonic

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K253254 2026-01-28
K190124 2019-10-20
K191079 2019-08-16
K140990 2015-02-27
K132445 2013-12-06
K132443 2013-11-22
K110173 2011-04-07
K093723 2010-09-08
K093000 2010-07-30
K050710 2005-03-30

Recalls

3 of these are 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
2024-03-13 Class II Process control Received complaints that bottles assembled with one batch of bottle collars can be disassembled in two parts when used under pressure (during treatment or storage if the use is not releasing the pressure inside the bottles). 342
2024-03-13 Class II Process control Received complaints that bottles assembled with one batch of bottle collars can be disassembled in two parts when used under pressure (during treatment or storage if the use is not releasing the pressure inside the bottles). 462
2024-03-13 Class II Process control Received complaints that bottles assembled with one batch of bottle collars can be disassembled in two parts when used under pressure (during treatment or storage if the use is not releasing the pressure inside the bottles). 54

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