X-Twist Biocomposite Suture Anchor

X-Twist Biocomposite Suture Anchor 4.75mm

Registry build 21.09.26
2manufacturers in China registered for this device type
9catalogue numbers in this listing
3510(k) clearances naming this product code

Who Else Makes It

All of them in Shanghai.

Chinese manufacturers registered for FDA product code MAI
Manufacturer City Province Registered as Device types
Zimmer (Shanghai) Medical International Trading Co., Ltd. Shanghai Shanghai Exporter 106
Arthrex (Shanghai) Co., Ltd. Shanghai Shanghai Exporter 38

Record

Regulatory record for X-Twist Biocomposite Suture Anchor
Listed by Parcus Medical, LLC, United States
FDA product code MAI
Device type Fastener, Fixation, Biodegradable, Soft Tissue
Device class Class 2
Regulation 21 CFR 888.3030
Record published 2025-04-29
Record revised 2025-09-17 (version 2)

Specifications

Specifications
MRI safety MR Safe
Supplied sterile Yes
Single use Yes
Prescription Prescription only
Label carries lot or batch number, expiry date, manufacturing date

Catalogue Numbers

Catalogue numbers for X-Twist Biocomposite Suture Anchor
Catalogue number Size Status
XT44701 In distribution
XT46200 In distribution
XT44703 In distribution
XT45503 In distribution
XT45501 In distribution
XT44702 In distribution
XT45502 In distribution
XT45500 In distribution
XT44700 In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Arthrex® Arthrex, Inc. 545
Fix2Lock Osteonic Co., Ltd. 118
Delta Stryker Leibinger Gmbh & Co. KG 110
Reunite Screw System Biomet Orthopedics 85
ComposiTCP S.B.M 61
ActivaScrew™ Interference Bioretec Ltd. 54
Ligafix S.B.M 40
Twinfix Smith & Nephew, Inc. 28
Biosure Smith & Nephew, Inc. 27
TorqLoc Interference Bioretec Ltd. 27
FiberFIX Nanova BIO Materials Inc 25
AlphaVent Stryker GmbH 23

Showing 12 of 176. All products under Fastener, Fixation, Biodegradable, Soft Tissue

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K232513 2023-09-18
K192824 2019-11-02
K183501 2019-03-15

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