Who else makes this device?

Name: Suture USP 0
Brand: Suture USP 0

General & Plastic Surgery › SurgicalSuture, Surgical, Absorbable, Polydioxanone

Suture USP 0

Catalogue number BOM 1055S rev 05 Suture PDO USP 0 - Ster, listed by Suturion AB, Sweden, under Suture, Surgical, Absorbable, Polydioxanone. 2 manufacturers in China are registered for this product code.

Registry build 21.09.26

2manufacturers in China registered for this device type

1catalogue number

2510(k) clearances naming this product code

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 Suture USP 0
Listed by	Suturion AB, Sweden
FDA product code	NEW
Device type	Suture, Surgical, Absorbable, Polydioxanone
Device class	Class 2
Regulation	21 CFR 878.4840
Establishment	Specification developer, Complaint-file establishment, Manufacturer
510(k)	K250977
Record published	2025-12-15

Specifications

Specifications
MRI safety	Labeling does not contain MRI Safety Information
Sterilisation	Ethylene Oxide
Supplied sterile	Yes
Single use	Yes
Prescription	Prescription only
Label carries	lot or batch number, expiry date, manufacturing date

Catalogue Numbers

Catalogue numbers for Suture USP 0
Catalogue number	Size	Per pack	Status
BOM 1055S rev 05 Suture PDO USP 0 – Sterilized		12	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

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance	Decision date
K250977	2025-04-28
K242835	2025-01-22

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.