Unify Silk Surgical Sutures

UNIFY Silk Surgical Sutures, XXL 1, 40mm 3/8 circle Rev Cut, 30"

Registry build 21.09.26
3manufacturers in China registered for this device type
1catalogue number

Who Else Makes It

Concentrated in Shandong (2), Beijing (1).

Chinese manufacturers registered for FDA product code GAR
Manufacturer City Province Registered as Device types
Shandong Haidike Medical Products Co., Ltd. Heze Shandong 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 Unify Silk Surgical Sutures
Listed by Applied Dental, Inc.
FDA product code GAR
Device type Suture, Nonabsorbable, Synthetic, Polyamide
Device class Class 2
Regulation 21 CFR 878.5020
Record published 2015-08-19
Record revised 2021-02-05 (version 4)

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 Box of 12, case of 100

Catalogue Numbers

Catalogue numbers for Unify Silk Surgical Sutures
Catalogue number Size Status
XXL-1N30R40 In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
DemeLON Demetech Corp. 1,800
Dafilon B Braun Surgical SA 592
WEGO-Nylon Non-absorbable Surgical Suture With Needle Foosin Medical Supplies Inc.ltd 279
Ethilon Ethicon, Inc. 272
Monosof Covidien LP 256
DemeLON Multi Demetech Corp. 227
Surgilon Covidien LP 135
Atramat Internacional Farmacéutica S.A DE C.V 127
Supramid Extra S. Jackson, Inc. 119
Mani Sutures Nylon Mani, Inc. 88
Onatec Surgical Specialties México, S. de R.L. de C.V. 75
Sharpoint Plus Surgical Specialties México, S. de R.L. de C.V. 73

Showing 12 of 284. All products under Suture, Nonabsorbable, Synthetic, Polyamide

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
N85060 1988-02-22 NONABSORBABLE SURG. SUTURES, NYLON Deknatel, Inc.
N85316 1986-06-20 ETHILON/NUROLON NYLON SUTURES Ethicon, Inc.
N80838 1985-07-23 SUPRAMID EXTRA SUTURES S. Jackson, Inc.
N83511 1982-05-18 NON-ABSORBABLE SUTURES NYLON 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