Activbraid

ACTIVBRAID is a partially absorbable surgical co-braid suture indicated for soft-tissue approximation or ligation. The filing describes a combination of nonabsorbable…

Registry build 21.09.26

ACTIVBRAID is a partially absorbable surgical co-braid suture indicated for soft-tissue approximation or ligation. The filing describes a combination of nonabsorbable ultra-high-molecular-weight polyethylene and absorbable bovine-derived type I collagen.

The suture is available in several sizes and precut lengths, with or without needles, and its ends are stiffened with cyanoacrylate. The FDA summary also provides material resorption and strength-retention data from testing over specified periods.

Listed Item

ActivBraid 1.5mm Collagen-UHMWPE Co-Braid Suture Tape with 48mm 1/2c Taper Point Needle, White/Black, 36” (91.5cm)

Construction and Test Data

The FDA summary reports approximately 85 percent of original strength remaining at 16 weeks after implantation, with collagen absorption complete between 8 and 16 weeks. It also lists testing of tensile strength and knot security.

6manufacturers in China registered for this device type
14catalogue numbers in this listing
1510(k) clearance

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 Activbraid
Listed by Embody, Inc., United States
FDA product code GAT
Device type Suture, Nonabsorbable, Synthetic, Polyethylene
Device class Class 2
Regulation 21 CFR 878.5000
Establishment Manufacturer
510(k) K223822
Record published 2023-08-31
Record revised 2025-12-18 (version 5)

Specifications

Specifications
MRI safety MR Safe
Supplied sterile Yes
Single use Yes
Prescription Prescription only
Label carries lot or batch number, expiry date
Packaging Pack of 12, pack of 6

Catalogue Numbers

Catalogue numbers for Activbraid
Catalogue number Size Status
AB-150T-1B In distribution
AB-021R-1B In distribution
AB-250T-0W In distribution
AB-200R-1B In distribution
AB-200R-1W In distribution
AB-150T-2B In distribution
AB-150T-1W In distribution
AB-200R-2W In distribution
AB-021R-2B In distribution
AB-150T-2W In distribution
AB-200R-2B In distribution
AB-150T-0B In distribution
AB-250T-0B In distribution
AB-150T-0W 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
K223822 2023-06-02

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