XBraid S

Suture Shuttle

Registry build 21.09.26
6manufacturers in China registered for this device type
67catalogue numbers in this listing
7510(k) clearances naming this product code

Who Else Makes It

Concentrated in Shanghai (2), Shandong (2), Fujian (1).

Chinese manufacturers registered for FDA product code GAT
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
Shandong Haidike Medical Products Co., Ltd. Heze Shandong Manufacturer 22
Xiamen Zhiyuan Medical Technology Co., Ltd. Xiamen Fujian Contract manufacturer 22
Foosin Medical Supplies Inc.ltd Weihai Shandong Manufacturer 8
ARC Medical Supplies (Beijing) Co., Ltd. Beijing Beijing Manufacturer 7

Record

Regulatory record for XBraid S
Listed by Riverpoint Medical LLC, United States
FDA product code GAT
Device type Suture, Nonabsorbable, Synthetic, Polyethylene
Device class Class 2
Regulation 21 CFR 878.5000
Establishment Contract manufacturer, Specification developer, Complaint-file establishment, Manufacturer
Record published 2020-02-05
Record revised 2023-06-02 (version 3)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Supplied sterile Yes
Single use Yes
Label carries lot or batch number, expiry date, manufacturing date
Packaging Pack of 12, pack of 6

Catalogue Numbers

Catalogue numbers for XBraid S
Catalogue number Size Status
3910-900-027 In distribution
3910-900-034S In distribution
3910-900-060S In distribution
3910-900-028S In distribution
3910-900-061 In distribution
3910-900-062 In distribution
3910-900-126S In distribution
3910-900-025 In distribution
3910-900-037 In distribution
3910-900-063S In distribution
3910-900-120 In distribution
3910-900-028 In distribution
3910-900-121S In distribution
3910-900-133S In distribution
3910-900-127 In distribution
3910-900-116 In distribution
3910-900-111 In distribution
3910-900-023S In distribution
3910-900-042 In distribution
3910-900-122 In distribution
3910-900-127S In distribution
3910-900-126 In distribution
3910-900-060 In distribution
3910-900-123S In distribution
3910-900-061S In distribution
3910-900-143 In distribution
3910-900-040 In distribution
3910-900-062S In distribution
3910-900-027S In distribution
3910-900-038 In distribution
3910-900-029S In distribution
3910-900-036 In distribution
3910-900-039S In distribution
3910-900-041S In distribution
3910-900-026 In distribution
3910-900-122S In distribution
3910-900-037S In distribution
3910-900-034 In distribution
3910-900-035 In distribution
3910-900-033 In distribution
3910-900-033S In distribution
3910-900-131 In distribution
3910-900-030 In distribution
3910-900-123 In distribution
3910-900-026S In distribution
3910-900-042S In distribution
3910-900-023 In distribution
3910-900-041 In distribution
3910-900-039 In distribution
3910-900-121 In distribution
3910-900-036S In distribution
3910-900-063 In distribution
3910-900-120S In distribution
3910-900-025S In distribution
3910-900-052 In distribution
3910-900-131S In distribution
3910-900-029 In distribution
3910-900-111S In distribution
3910-900-038S In distribution
3910-900-110 In distribution
3910-900-040S In distribution
3910-900-052S In distribution
3910-900-116S In distribution
3910-900-110S In distribution
3910-900-035S In distribution
3910-900-133 In distribution
3910-900-030S In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Premicron B Braun Surgical SA 1,377
Deknatel Teleflex Medical LLC 1,198
FlexiGRAFT® LifeNet Health 992
DemeBOND Demetech Corp. 939
Ti-Cron Covidien LP 482
HS FIber Riverpoint Medical LLC 413
Ethibond Excel Ethicon, Inc. 383
Arthrex® Arthrex, Inc. 307
Dagrofil B Braun Surgical SA 195
WEGO-Polyester Nonabsorbable Surgical Suture With Needle Foosin Medical Supplies Inc.ltd 175
Cardioxyl ® Peters Surgical 162
Silkam B Braun Surgical SA 150

Showing 12 of 275. All products under Suture, Nonabsorbable, Synthetic, Polyethylene

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K253024 2025-10-16
K252201 2025-08-13
K231163 2024-01-05
K202242 2020-09-10
K190817 2019-05-01
K153307 2016-02-12
K100006 2010-05-10

PMA Approvals

A premarket approval is the full Class III route, granted on clinical evidence rather than on equivalence to an existing device. It is the highest regulatory bar a device of this type can clear.

FDA premarket approvals naming this product code
PMA number Decision Trade name Approved to
N16374 1986-01-23 PROLENE*POLYPROPYLENE SUTURE NONABSORBABLE SURG. S Ethicon, Inc.
P810028 1984-12-17 DEKLENE(TM) Deknatel, Inc.
N17825 1981-09-24 SURGILENE Davis & Geck, Inc.

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