Synth™ Plus Bilateral

HC Biologics Private Label(MPB1-B1T1N10-15S)

Registry build 21.09.26
21manufacturers in China registered for this device type
48catalogue numbers in this listing
2510(k) clearances naming this product code

Who Else Makes It

Concentrated in Shanghai (7), Jiangsu (6), Guangdong (5). 6 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code HRX
Manufacturer City Province Registered as Device types
Modern Medical Equipment Manufacturing Ltd. Heng Li, Dongguan Guangdong Contract manufacturer 26
Dongguan BAO Kang Dian ZI KE JI Limited Dongguan Guangdong Contract manufacturer 24
Sanmina Kunshan Jiangsu Contract manufacturer 15
Peter’s Technology (Suzhou) Co., Ltd. Suzhou Jiangsu Contract manufacturer 9
Jiangsu Shenli Medical Production Co., Ltd. Changzhou Jiangsu Contract manufacturer 6
PAN-International Precision Electronic Co., Ltd. Dongguan Guangdong Contract manufacturer 4
Zimmer (Shanghai) Medical International Trading Co., Ltd. Shanghai Shanghai Exporter 106
Shanghai JPY ION-Tech Co., Ltd. Shanghai Shanghai Contract manufacturer 70
Medtronic (Changzhou) Medical Devices Technology Co., Ltd. Changzhou Jiangsu Manufacturer 53
Hangzhou Fushan Medical Appliance Co., Ltd. Hangzhou Zhejiang Contract manufacturer 44
Arthrex (Shanghai) Co., Ltd. Shanghai Shanghai Exporter 38
Goals Sterilization Co., Ltd. Jiaxing Zhejiang Contract manufacturer 26

Showing 12 of 21. All 21 manufacturers in China registered for Arthroscope

Record

Regulatory record for Synth™ Plus Bilateral
Listed by Imedicom Co., Ltd., South Korea
FDA product code HRX
Device type Arthroscope
Device class Class 2
Regulation 21 CFR 888.1100
Establishment Manufacturer, Exporter
510(k) K182287
Record published 2024-03-25

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Supplied sterile Yes
Single use Yes
Prescription Prescription only
Latex Contains natural rubber latex
Label carries lot or batch number, expiry date, manufacturing date

Catalogue Numbers

Catalogue numbers for Synth™ Plus Bilateral
Catalogue number Size Status
SYNTH-SPB31 In distribution
SYNTH-SPB5 In distribution
SYNTH-SPB18 In distribution
SYNTH-SPB15 In distribution
SYNTH-SPB14 In distribution
SYNTH-SPB40 In distribution
SYNTH-SPB12 In distribution
SYNTH-SPB3 In distribution
SYNTH-SPB47 In distribution
SYNTH-SPB32 In distribution
SYNTH-SPB26 In distribution
SYNTH-SPB7 In distribution
SYNTH-SPB30 In distribution
SYNTH-SPB46 In distribution
SYNTH-SPB43 In distribution
SYNTH-SPB41 In distribution
SYNTH-SPB36 In distribution
SYNTH-SPB19 In distribution
SYNTH-SPB11 In distribution
SYNTH-SPB2 In distribution
SYNTH-SPB44 In distribution
SYNTH-SPB10 In distribution
SYNTH-SPB23 In distribution
SYNTH-SPB45 In distribution
SYNTH-SPB4 In distribution
SYNTH-SPB21 In distribution
SYNTH-SPB38 In distribution
SYNTH-SPB34 In distribution
SYNTH-SPB8 In distribution
SYNTH-SPB24 In distribution
SYNTH-SPB33 In distribution
SYNTH-SPB16 In distribution
SYNTH-SPB9 In distribution
SYNTH-SPB13 In distribution
SYNTH-SPB22 In distribution
SYNTH-SPB35 In distribution
SYNTH-SPB17 In distribution
SYNTH-SPB1 In distribution
SYNTH-SPB6 In distribution
SYNTH-SPB37 In distribution
SYNTH-SPB In distribution
SYNTH-SPB25 In distribution
SYNTH-SPB29 In distribution
SYNTH-SPB39 In distribution
SYNTH-SPB27 In distribution
SYNTH-SPB28 In distribution
SYNTH-SPB42 In distribution
SYNTH-SPB20 In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Surgical Direct Surgical Direct, Inc. 299
Arthroscope Karl Storz GmbH & Co. KG 278
Conmed/Linvatec Provision 265
Arthroscope Smith & Nephew, Inc. 255
Medline Medline Industries, Inc. 205
Arthroscope Sterilmed, Inc. 184
Sustainable Technologies Provision 150
Medline Renewal Medline Industries, Inc. 123
Stryker Provision 113
Arthrex® Arthrex, Inc. 109
Arthrex Provision 109
Eberle Eberle GmbH & Co. KG 92

Showing 12 of 567. All products under Arthroscope

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K182287 2019-04-06
K151268 2016-03-16

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