Ptfe

9 catalogue numbers from 5067-698, listed by Riverpoint Medical LLC, United States, under Suture, Surgical, Nonabsorbable, Expanded, Polytetraflouroethylene. 1 manufacturer in China is registered for this product code.

Registry build 21.09.26
1manufacturer
9catalogue numbers in this listing
1510(k) clearance

Who Else Makes It

Registered in Shandong.

Chinese manufacturers registered for FDA product code NBY
Manufacturer City Province Registered as Device types
Foosin Medical Supplies Inc.ltd Weihai Shandong Manufacturer 8

Record

Regulatory record for Ptfe
Listed by Riverpoint Medical LLC, United States
FDA product code NBY
Device type Suture, Surgical, Nonabsorbable, Expanded, Polytetraflouroethylene
Device class Class 2
Regulation 21 CFR 878.5035
Establishment Contract manufacturer, Specification developer, Complaint-file establishment, Manufacturer
Record published 2016-09-29
Record revised 2018-03-29 (version 2)

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
Packaging Pack of 12

Catalogue Numbers

Catalogue numbers for Ptfe
Catalogue number Size Status
5067-698 In distribution
5067-581 In distribution
T8682 In distribution
6067-661 In distribution
5067-705 In distribution
5067-652 In distribution
5067-714 In distribution
5067-643 In distribution
5067-670 In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Demetech PTFE Demetech Corp. 201
Biotex Purgo Biologics Inc. 60
Sterile PTFE Surgical Suture Omnia Medical 45
Monotex Riverpoint Medical LLC 36
Cytoplast™ PTFE Suture Osteogenics Biomedical, Inc. 34
Darby Dental Supply, LLC Darby Dental Supply, LLC 24
Cytosurg Riverpoint Medical LLC 18
Unify PTFE Surgical Sutures Applied Dental, Inc. 13
Klosure Riverpoint Medical LLC 10
Gibson Benco Dental Supply Co. 9
Maxima Henry Schein, Inc. 9
Golnit PTFE Suture Golnit Sutures 9

Showing 12 of 34. All products under Suture, Surgical, Nonabsorbable, Expanded, Polytetraflouroethylene

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K140415 2014-03-26

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