CoNextions TR Tendon Repair System-Implant Mechanism

Catalogue number FA0004, listed by Conextions Inc, United States, under Suture, Nonabsorbable, Steel, Monofilament And Multifilament, Sterile. 1 manufacturer in China is registered for this product code.

Registry build 21.09.26
1manufacturer
1catalogue number
1510(k) clearance

Who Else Makes It

Registered in Shandong.

Chinese manufacturers registered for FDA product code GAQ
Manufacturer City Province Registered as Device types
Foosin Medical Supplies Inc.ltd Weihai Shandong Manufacturer 8

Record

Regulatory record for CoNextions TR Tendon Repair System-Implant Mechanism
Listed by Conextions Inc, United States
FDA product code GAQ
Device type Suture, Nonabsorbable, Steel, Monofilament And Multifilament, Sterile
Device class Class 2
Regulation 21 CFR 878.4495
Establishment Complaint-file establishment, Manufacturer
510(k) K203855
Record published 2022-04-28
Record revised 2023-08-31 (version 2)

Specifications

Specifications
MRI safety MR Conditional
Supplied sterile Yes
Single use Yes
Prescription Prescription only
Label carries lot or batch number, expiry date, manufacturing date
Packaging 1 of 10

Catalogue Numbers

Catalogue numbers for CoNextions TR Tendon Repair System-Implant Mechanism
Catalogue number Size Status
FA0004 In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Ethibond Excel Ethicon, Inc. 175
DemeSTEEL Demetech Corp. 150
Deknatel Teleflex Medical LLC 94
Ethicon Ethicon, Inc. 73
Steel Covidien LP 44
Acier Peters Surgical 43
E-Pack Ethicon, Inc. 17
Ethi-PAK Ethicon, Inc. 11
Steel Wire Resorba Medical GmbH 10
Steelex B Braun Surgical SA 7
Valkyrie Surgical Specialties México, S. de R.L. de C.V. 6
Fumedica Surgical Specialties México, S. de R.L. de C.V. 6

Showing 12 of 26. All products under Suture, Nonabsorbable, Steel, Monofilament And Multifilament, Sterile

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K203855 2022-04-22

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