McKesson

Suture, Pediex 1 96" LP48" VIO

Registry build 21.09.26
2manufacturers in China registered for this device type
16catalogue numbers in this listing

Who Else Makes It

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

Chinese manufacturers registered for FDA product code NEW
Manufacturer City Province Registered as Device types
Foosin Medical Supplies Inc.ltd Weihai Shandong Manufacturer 8
ARC Medical Supplies (Beijing) Co., Ltd. Beijing Beijing Manufacturer 7

Record

Regulatory record for McKesson
Listed by Mckesson Medical-Surgical Inc.
FDA product code NEW
Device type Suture, Surgical, Absorbable, Polydioxanone
Device class Class 2
Regulation 21 CFR 878.4840
510(k) K172659
Record published 2026-05-21

Specifications

Specifications
MRI safety MR Safe
Supplied sterile Yes
Single use Yes
Prescription Prescription only
Latex Labelled latex-free
Label carries lot or batch number, expiry date, manufacturing date
Packaging Case of 24

Catalogue Numbers

Catalogue numbers for McKesson
Catalogue number Size Per pack Status
M-Z496G 12 In distribution
M-Z416H 36 In distribution
M-Z340H 36 In distribution
M-Z333H 36 In distribution
M-Z259H 36 In distribution
M-Z346H 36 In distribution
M-Z497G 12 In distribution
M-Z493G 12 In distribution
M-Z303H 36 In distribution
M-Z423H 36 In distribution
M-Z317H 36 In distribution
M-Z494G 12 In distribution
M-Z339H 36 In distribution
M-Z880G 12 In distribution
M-Z463G 12 In distribution
M-Z443H 36 In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
DemeDIOX Demetech Corp. 994
Monoplus B Braun Surgical SA 697
PDS Ethicon, Inc. 430
Wego-PDO Absorbable Surgical Suture With Needle Foosin Medical Supplies Inc.ltd 180
Stratafix Ethicon, Inc. 172
Atramat Internacional Farmacéutica S.A DE C.V 74
PDO Max Threads Max Pdo Inc 64
Assufil Monofilamento Assut Europe 50
LES Encres Meditime Co., Ltd. 42
DemeDIOX Barbed Demetech Corp. 40
Viola Meditime Co., Ltd. 36
Stratafix Spiral Surgical Specialties México, S. de R.L. de C.V. 34

Showing 12 of 292. All products under Suture, Surgical, Absorbable, Polydioxanone

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
N18331 1986-06-06 PDS SUTURE (DYED) Ethicon, 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