Surgicel SNoW

Surgicel Absorbable Hemostat, Structured Non-Woven Fabric

Registry build 21.09.26
2manufacturers in China registered for this device type
6catalogue numbers in this listing
2recalls on this code

Who Else Makes It

Concentrated in Shanghai (1), Beijing (1). One is registered as a contract manufacturer, able to build to a specification.

Chinese manufacturers registered for FDA product code LMG
Manufacturer City Province Registered as Device types
Beijing Huan QIU LI Kang Biotech Co., Ltd. Beijing Beijing Contract manufacturer 2
Sterigenics Shanghai E Beam Ltd. Shanghai Shanghai Contract manufacturer 14

Record

Regulatory record for Surgicel SNoW
Listed by Ethicon, Inc., United States
FDA product code LMG
Device type Agent, Absorbable Hemostatic, Non-Collagen Based
Device class Class 3
Regulation 21 CFR 878.4490
Establishment Contract manufacturer, Specification developer, Manufacturer, Exporter
510(k) N12159
Record published 2014-09-20
Record revised 2025-11-18 (version 11)

Specifications

Specifications
MRI safety MR Safe
Supplied sterile Yes
Single use Yes
Prescription Prescription only
Label carries lot or batch number, expiry date
Storage Storage environment temperature 15 to 30 °C
Packaging Case of 10, box of 10

Catalogue Numbers

Catalogue numbers for Surgicel SNoW
Catalogue number Size Status
2092 In distribution
2082 In distribution
2093 In distribution
2091 In distribution
2083 In distribution
2081 In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Surgicel Ethicon Sàrl 8
Surgicel NU-Knit Ethicon Sàrl 6
Arista Davol Inc. 6
Surgicel Fibrillar Ethicon, Inc. 5
PerClot Baxter Healthcare Corporation 5
Emergency Medical Products Emergency Medical Products, Inc. 3
Veriset Covidien LP 3
Surgicel Fibrillar Ethicon Sàrl 3
Surgicel Ethicon, Inc. 1
Tabotamp Fibrillar Ethicon, Inc. 1
Ethicon Ethicon, Inc. 1

Recalls

2 of these are Class II. Class II means a temporary or reversible health consequence. Volume alone is not a quality signal: a manufacturer that ships more recalls more.

Recalls referencing this product code
Initiated FDA class Root cause Reason Quantity
2024-06-11 Class II Process control Some foil pouches were found torn open, impacting the sterile barrier which was traced to a specific machine used during product packaging. 450,793 units (65,950 US, 384,843 OUS)
2024-06-11 Class II Process control Some foil pouches were found torn open, impacting the sterile barrier which was traced to a specific machine used during product packaging. 39,010 units (All US)

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
P210036 2023-05-19 PerClot® Polysaccharide Hemostatic System Baxter Healthcare Corporation
N12159 2023-04-04 SURGICEL® Absorbable Hemostats (SURGICEL® POWDER™) Ethicon, Inc.
P050038 2012-03-23 ARISTA AH ABSORBABLE HEMOSTAT Davol Inc.
N5798 1991-02-08 OXYCELL Bd Becton Dickinson Vacutainer Systems Preanalytic

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