Monocryl

Antibacterial Violet Monofilament (Poliglecaprone 25), Absorbable Surgical Suture

Registry build 21.09.26
4manufacturers in China registered for this device type
128catalogue numbers in this listing
27510(k) clearances naming this product code
21recalls on this code

Who Else Makes It

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

Chinese manufacturers registered for FDA product code GAM
Manufacturer City Province Registered as Device types
Zimmer (Shanghai) Medical International Trading Co., Ltd. Shanghai Shanghai Exporter 106
Foosin Medical Supplies Inc.ltd Weihai Shandong Manufacturer 8
ARC Medical Supplies (Beijing) Co., Ltd. Beijing Beijing Manufacturer 7
Sichuan Innovation Technology Co., Ltd. Chengdu Sichuan Contract manufacturer 2

Record

Regulatory record for Monocryl
Listed by Ethicon, Inc., United States
FDA product code GAM
Device type Suture, Absorbable, Synthetic, Polyglycolic Acid
Device class Class 2
Regulation 21 CFR 878.4493
Establishment Contract manufacturer, Specification developer, Manufacturer, Exporter
510(k) K960653
Record published 2015-09-01
Record revised 2025-12-02 (version 8)

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 up to 30 °C; Storage environment temperature up to 86 °F
Packaging Box of 36, box of 12, box of 24
Distribution end date 2017-09-11

Catalogue Numbers

Catalogue numbers for Monocryl
Catalogue number Size Status
Y318H In distribution
D9936 In distribution
Y47T In distribution
Y911G In distribution
D9543 In distribution
Y4214H In distribution
Y351H In distribution
MCP605H In distribution
MCP496G In distribution
D9924 In distribution
Y464G In distribution
Y701D In distribution
MCP834G In distribution
MCP682H In distribution
MCP507G In distribution
Y352H In distribution
MCP347H In distribution
MCP304H In distribution
MCPB946H In distribution
MCP426H In distribution
D9639 In distribution
MCP944H In distribution
Y771D In distribution
Y334H In distribution
MCP345H In distribution
MCP339H In distribution
YY31D In distribution
MCP492G In distribution
Y436H In distribution
Y341H In distribution
MCP317H In distribution
Y48G In distribution
MCP344H In distribution
Y317H In distribution
MCP266H In distribution
MCP936H In distribution
Y907G In distribution
Y605H In distribution
MCP823G In distribution
D10101 In distribution
Y304H In distribution
Y604H In distribution
YB257H In distribution
MCP946H In distribution
D9555 In distribution
Y315H In distribution
Y339H In distribution
YY70D In distribution
MCP942H In distribution
Y606H In distribution
MCPB944H In distribution
MCP967H In distribution
MCP513G In distribution
MCP922H In distribution
Y908G In distribution
MCP895H In distribution
MCP416H In distribution
MCP923H In distribution
Y527H In distribution
MCP604H In distribution
YY30D In distribution
Y740D In distribution
D9503 In distribution
MCP358H In distribution
MCP935H In distribution
YY31G In distribution
D10041 In distribution
D9954 In distribution
D10100 In distribution
MCP427H In distribution
MCP957H In distribution
D9213 In distribution
MCP835G In distribution
YB258 In distribution
MCP415H In distribution
MCP822G In distribution
Y303H In distribution
MCP333H In distribution
D9937 In distribution
YY71D In distribution
MCP489G In distribution
MCP844G In distribution
MCP495G In distribution
MCPB945H In distribution
Y316H In distribution
MCP494G In distribution
MCP943G In distribution
MCP377H In distribution
MCP315H In distribution
MCP845G In distribution
Y942G In distribution
D9923 In distribution
MCP214H In distribution
MCP463G In distribution
MCPB316H In distribution
MCP523H In distribution
Y463G In distribution
D10062 In distribution
Y922H In distribution
D10197 In distribution
Y305H In distribution
D9842 In distribution
MCP316H In distribution
MCP923G In distribution
MCP2543G In distribution
MCP213H In distribution
Y340H In distribution
MCPB416H In distribution
Y357H In distribution
MCP987H In distribution
Y346H In distribution
MCP947H In distribution
MCP497G In distribution
MCP945H In distribution
MCP493G In distribution
Y399H In distribution
MCPB346H In distribution
MCP417H In distribution
Y344H In distribution
MCP173H In distribution
MCP942G In distribution
MCP943H In distribution
D9568 In distribution
MCP346H In distribution
D9925 In distribution
MCP340H In distribution
MCP490G In distribution
MCPB345H Withdrawn

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Novosyn B Braun Surgical SA 2,286
DemeCRYL Demetech Corp. 2,092
DemeSORB Demetech Corp. 1,625
Safil B Braun Surgical SA 1,613
Monosyn B Braun Surgical SA 1,096
E-Pack Ethicon, Inc. 967
Coated Vicryl Ethicon, Inc. 933
DemeQUICK Demetech Corp. 732
Polysorb Covidien LP 732
DemeCAPRONE Demetech Corp. 707
Wego-PGA Absorbable Surgical Suture With Needle Foosin Medical Supplies Inc.ltd 554
Safil Quick+ B Braun Surgical SA 414

Showing 12 of 463. All products under Suture, Absorbable, Synthetic, Polyglycolic Acid

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K253394 2026-06-25
K253852 2026-02-06
K252743 2025-12-22
K221744 2022-11-15
K201996 2020-12-21
K192580 2019-12-18
K183183 2019-06-27
K181652 2018-09-28
K161726 2016-07-12
K153611 2016-06-03
K151200 2015-08-13
K142822 2015-03-26
K132580 2014-02-28
K050845 2005-06-29
K033746 2003-12-18
K032420 2003-10-22
K022715 2002-12-19
K022269 2002-09-13
K974299 1998-02-13
K970317 1997-04-25
K964345 1996-12-16
K962480 1996-08-02
K946271 1995-06-15
K944110 1995-01-18
K930772 1994-01-07
K930360 1993-12-17
K915835 1992-03-23

Recalls Naming This Product

5 recalls name this product by its own identifiers, the 510(k) it is cleared under.

Recalls naming the identifiers of Monocryl
Recalled by Identified by Initiated FDA class Root cause Reason Quantity Closed
Ethicon, Inc. 510(k) number 2024-10-08 Class II Process control Due a component mix-up in manufacturing, the affected products may contain incorrect needle type/size and suture length. 16,524 devices
Ethicon, Inc. 510(k) number 2024-05-10 Class II Under Investigation by firm Issue on a specific packaging machine resulted in a hole in the primary packaging, product sterility compromised and could result in infection. 306000 units
Ethicon, Inc. 510(k) number 2024-05-10 Class II Under Investigation by firm Issue on a specific packaging machine resulted in a hole in the primary packaging, product sterility compromised and could result in infection. 287892 units
Ethicon, Inc. 510(k) number 2009-02-02 Not classified Process control Sterility Issue: The firm decided to remove the product because it cannot assure the sterility of the products due to a failure in the sterilization process. 1,758,360 total 2009-10-21
Ethicon, Inc. 510(k) number 2009-02-02 Not classified Process control Sterility Issue: The firm decided to remove the product because it cannot assure the sterility of the products due to a failure in the sterilization process. 1,758,360 total 2009-10-21

Recalls

11 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 Closed
2024-09-25 Class II Under Investigation by firm Complaints were received regarding needle pull-off and suture degradation. Analysis on returned product from this lot confirmed that some sutures were visually degraded in the package. 31,032 units
2024-05-10 Class II Under Investigation by firm Issue on a specific packaging machine resulted in a hole in the primary packaging, product sterility compromised and could result in infection. 341532 units
2024-05-10 Class II Under Investigation by firm Issue on a specific packaging machine resulted in a hole in the primary packaging, product sterility compromised and could result in infection. 56952 units
2024-05-10 Class II Under Investigation by firm Issue on a specific packaging machine resulted in a hole in the primary packaging, product sterility compromised and could result in infection. 55296 units
2024-03-08 Class II Under Investigation by firm Degraded and unusable upon removal from the foil pouch due to exposed environmental conditions during transit and storage, compromising sterility 395 units
2022-09-20 Class II Under Investigation by firm Packages may contain a PS-1 cutting edge needle and not the intended SH taper point needle may result in more tissue trauma than is anticipated for taper point needles, which may necessitate repair 2,280 eaches
2022-03-24 Class II Employee error Affected product lots may contain the incorrect needle type/size and suture length due to component mix-up. 2808 (all OUS)
2020-09-09 Class II Packaging process control Product in the foil package for VICRYL V960 may not match the foil label and sales unit carton. The correct VICRYL suture is size 10-0, 4 inches (10 cm) in length, has monofilament construction, and a single needle. The incorrect VICRYL sut 1,032 eaches (OUS only) 2023-11-07
2020-01-03 Class II Process control Some sutures in the lot may exhibit a small section of braid fraying, which can lead to reduced tensile strength at that point. 23688 units 2021-08-13
2019-03-12 Class II Packaging process control VICRYL Suture, VICRYL Plus Suture, PDS Suture- may contain product that does not match the sales unit carton and foil label. 550,681 eaches (WW) Total 2020-07-17
2017-08-17 Class II Equipment maintenance On August 17, 2017, Ethicon had decided to initiate a medical device recall
(removal) of the twenty-five (25) lots of VICRYL RAPIDETM (Polyglactin 910) Suture
that were distributed to the field. During finished goods testing, a suture damag
129,372 Eaches (Internationally) 2019-05-08
2010-04-20 Not classified Other Channels in the packaging seal that can lead to suture degradation and loss of packaging integrity. Recall Z-0021-2009 was initiated in 2008. Ethicon had decided to recall all sutures product during the may to June 2007 timeframe. 118332 eaches were sent to the US Distribution Center, of wh 2011-07-19
2009-02-02 Not classified Process control Sterility Issue: The firm decided to remove the product because it cannot assure the sterility of the products due to a failure in the sterilization process. 1,758,360 total 2009-10-21
2009-02-02 Not classified Process control Sterility Issue: The firm decided to remove the product because it cannot assure the sterility of the products due to a failure in the sterilization process. 1,758,360 total 2009-10-21
2009-02-02 Not classified Process control Sterility Issue: The firm decided to remove the product because it cannot assure the sterility of the products due to a failure in the sterilization process. 1,758,360 total 2009-10-21
2008-08-11 Not classified Packaging Package defect compromised the integrity of the primary seal, which could lead to premature suture degradation and/or impair the sterile barrier of the product. 6912 2012-06-05
2006-05-04 Not classified Other Misalignment of packaging sealing platform created open seals and/or open channels in the packaging seal causing degradation of the sutures. 1157 dozens 2007-12-17
2006-02-16 Not classified Other The unique absorption profile of Panacryl in the suture could act as a foreign body so that surgeons should consider its use in specific situations. 1,061,712 sutures 2006-12-07

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
P840051 1989-06-07 MAXON(TM) POLYGLYCONATE MONOFILAMENT ABSORBABLE SU Davis & Geck, Inc.
N18387 1987-06-18 PDS(TM) SUTURE (CLEAR) Ethicon, Inc.
N16881 1981-12-04 DEXON 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