IZI Fiber

4 catalogue numbers from HS116, listed by Riverpoint Medical LLC, United States, under Suture, Nonabsorbable, Synthetic, Polyethylene. 6 manufacturers in China are registered for this product code.

Registry build 21.09.26
6manufacturers in China registered for this device type
4catalogue 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 IZI Fiber
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 2026-06-30

Specifications

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

Catalogue Numbers

Catalogue numbers for IZI Fiber
Catalogue number Size Status
HS116 In distribution
HS159 In distribution
HS514 In distribution
HS125 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