Pronova

Blue Monofilament Poly(VDF and VDF-co-hexafluoropropylene), Nonabsorbable Surgical Suture

Registry build 21.09.26
3manufacturers in China registered for this device type
105catalogue numbers in this listing
4510(k) clearances naming this product code
22recalls on this code

Who Else Makes It

Concentrated in Shandong (2), Beijing (1).

Chinese manufacturers registered for FDA product code GAW
Manufacturer City Province Registered as Device types
Shandong Haidike Medical Products Co., Ltd. Heze Shandong Manufacturer 22
Foosin Medical Supplies Inc.ltd Weihai Shandong Manufacturer 8
ARC Medical Supplies (Beijing) Co., Ltd. Beijing Beijing Manufacturer 7

Record

Regulatory record for Pronova
Listed by Ethicon, Inc., United States
FDA product code GAW
Device type Suture, Nonabsorbable, Synthetic, Polypropylene
Device class Class 2
Regulation 21 CFR 878.5010
Establishment Contract manufacturer, Specification developer, Manufacturer, Exporter
510(k) K001625
Record published 2015-09-01
Record revised 2026-03-27 (version 9)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Supplied sterile Yes
Single use Yes
Prescription Prescription only
Label carries lot or batch number, expiry date
Storage Storage environment temperature up to 86 °F; Storage environment temperature up to 30 °C
Packaging Box of 36, box of 12
Distribution end date 2017-09-11

Catalogue Numbers

Catalogue numbers for Pronova
Catalogue number Size Status
3523H In distribution
3732LG In distribution
3557H In distribution
3580H In distribution
PNM3702 In distribution
PN3702H In distribution
M3805 In distribution
M3735 In distribution
3776H In distribution
3526H In distribution
3862H In distribution
M3743 In distribution
3581H In distribution
3717H In distribution
PN3706H In distribution
M3703 In distribution
PN584G In distribution
3556H In distribution
3725H In distribution
3975H In distribution
PN3805H In distribution
PN3557H In distribution
D10189 In distribution
PN489G In distribution
PN3701H In distribution
3842H In distribution
PN3711H In distribution
3321H In distribution
M3600 In distribution
M3725 In distribution
M3706 In distribution
3307H In distribution
D10027 In distribution
D9981 In distribution
PNM3706 In distribution
3805H In distribution
PN3710H In distribution
3709H In distribution
PN3523H In distribution
M3766 In distribution
PN3307H In distribution
M3767 In distribution
3702H In distribution
3701H In distribution
PN3580H In distribution
PNM3703 In distribution
3806H In distribution
PN3976H In distribution
D9998 In distribution
M3737 In distribution
3521H In distribution
3522H In distribution
PN3522H In distribution
M3770 In distribution
3711H In distribution
PNM3725 In distribution
3555H In distribution
3558H In distribution
PN3726H In distribution
M3747 In distribution
PN3725H In distribution
M3702 In distribution
3741LG In distribution
M3726 In distribution
PN3703H In distribution
3710H In distribution
PN3558H In distribution
3304H In distribution
PN3556H In distribution
3706H In distribution
PN3305H In distribution
M3720 In distribution
PNM3720 In distribution
PN496G In distribution
3730LG In distribution
M3739 In distribution
D9744 In distribution
PN3717H In distribution
M3753 In distribution
PN3735H In distribution
PN3581H In distribution
PN3741LG In distribution
D10086 In distribution
3707H In distribution
PNM3709 In distribution
D10114 In distribution
M3768 In distribution
M3709 In distribution
PN3762H In distribution
PN3806H In distribution
PN3526H In distribution
3976H In distribution
3703H In distribution
PN3321H In distribution
3720H In distribution
3762H In distribution
3735H In distribution
PN3709H In distribution
PN3720H In distribution
PNM3805 In distribution
3726H In distribution
3305H In distribution
M3304 Withdrawn
3861H Withdrawn
M3769 Withdrawn

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
DemeLENE Demetech Corp. 1,707
Premilene B Braun Surgical SA 1,247
Optilene B Braun Surgical SA 1,110
Prolene Ethicon, Inc. 765
Deknatel Teleflex Medical LLC 373
Corolene® Peters Surgical 354
WEGO-Polypropylene Nonabsorbable Surgical Suture With Needle Foosin Medical Supplies Inc.ltd 346
Surgipro II Covidien LP 254
Surgipro ll Covidien LP 152
Atramat Internacional Farmacéutica S.A DE C.V 140
Surgipro Covidien LP 133
Filaprop Meril Endo Surgery PVT. Ltd. 123

Showing 12 of 200. All products under Suture, Nonabsorbable, Synthetic, Polypropylene

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K253572 2026-03-27
K133356 2013-12-06
K001625 2000-07-10
K920437 1992-07-30

Recalls

22 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
2024-12-20 Class II Process control Sutures may have an open seal on the primary packaging, due to a manufacturing issue on a specific machine, and if issue is undetected could lead to breach in sterility, could introduce pathogens to the patient and cause infection. 15,948
2024-12-20 Class II Process control Sutures may have an open seal on the primary packaging, due to a manufacturing issue on a specific machine, and if issue is undetected could lead to breach in sterility, could introduce pathogens to the patient and cause infection. 48
2024-12-20 Class II Process control Sutures may have an open seal on the primary packaging, due to a manufacturing issue on a specific machine, and if issue is undetected could lead to breach in sterility, could introduce pathogens to the patient and cause infection. 78792
2018-05-07 Class II Package design/selection The needle associated with certain suture product codes has the potential to perforate the packaging due to a packaging design issue. A perforated package has the potential to cause a soft tissue injury to a healthcare
professional handling
456 2020-06-08
2018-05-07 Class II Package design/selection The needle associated with certain suture product codes has the potential to perforate the packaging due to a packaging design issue. A perforated package has the potential to cause a soft tissue injury to a healthcare
professional handling
15180 2020-06-08
2018-05-07 Class II Package design/selection The needle associated with certain suture product codes has the potential to perforate the packaging due to a packaging design issue. A perforated package has the potential to cause a soft tissue injury to a healthcare
professional handling
48 2020-06-08
2018-05-07 Class II Package design/selection The needle associated with certain suture product codes has the potential to perforate the packaging due to a packaging design issue. A perforated package has the potential to cause a soft tissue injury to a healthcare
professional handling
4440 2020-06-08
2018-05-07 Class II Package design/selection The needle associated with certain suture product codes has the potential to perforate the packaging due to a packaging design issue. A perforated package has the potential to cause a soft tissue injury to a healthcare
professional handling
1752 2020-06-08
2018-05-07 Class II Package design/selection The needle associated with certain suture product codes has the potential to perforate the packaging due to a packaging design issue. A perforated package has the potential to cause a soft tissue injury to a healthcare
professional handling
2844 2020-06-08
2018-05-07 Class II Package design/selection The needle associated with certain suture product codes has the potential to perforate the packaging due to a packaging design issue. A perforated package has the potential to cause a soft tissue injury to a healthcare
professional handling
3024 2020-06-08
2018-05-07 Class II Package design/selection The needle associated with certain suture product codes has the potential to perforate the packaging due to a packaging design issue. A perforated package has the potential to cause a soft tissue injury to a healthcare
professional handling
300 2020-06-08
2018-05-07 Class II Package design/selection The needle associated with certain suture product codes has the potential to perforate the packaging due to a packaging design issue. A perforated package has the potential to cause a soft tissue injury to a healthcare
professional handling
276 2020-06-08
2018-05-07 Class II Package design/selection The needle associated with certain suture product codes has the potential to perforate the packaging due to a packaging design issue. A perforated package has the potential to cause a soft tissue injury to a healthcare
professional handling
552 2020-06-08
2018-05-07 Class II Package design/selection The needle associated with certain suture product codes has the potential to perforate the packaging due to a packaging design issue. A perforated package has the potential to cause a soft tissue injury to a healthcare
professional handling
516 2020-06-08
2018-05-07 Class II Package design/selection The needle associated with certain suture product codes has the potential to perforate the packaging due to a packaging design issue. A perforated package has the potential to cause a soft tissue injury to a healthcare
professional handling
4968 2020-06-08
2018-05-07 Class II Package design/selection The needle associated with certain suture product codes has the potential to perforate the packaging due to a packaging design issue. A perforated package has the potential to cause a soft tissue injury to a healthcare
professional handling
588 2020-06-08
2018-05-07 Class II Package design/selection The needle associated with certain suture product codes has the potential to perforate the packaging due to a packaging design issue. A perforated package has the potential to cause a soft tissue injury to a healthcare
professional handling
1728 2020-06-08
2018-05-07 Class II Package design/selection The needle associated with certain suture product codes has the potential to perforate the packaging due to a packaging design issue. A perforated package has the potential to cause a soft tissue injury to a healthcare
professional handling
1020 2020-06-08
2018-05-07 Class II Package design/selection The needle associated with certain suture product codes has the potential to perforate the packaging due to a packaging design issue. A perforated package has the potential to cause a soft tissue injury to a healthcare
professional handling
432 2020-06-08
2018-05-07 Class II Package design/selection The needle associated with certain suture product codes has the potential to perforate the packaging due to a packaging design issue. A perforated package has the potential to cause a soft tissue injury to a healthcare
professional handling
144 2020-06-08
2018-05-07 Class II Package design/selection The needle associated with certain suture product codes has the potential to perforate the packaging due to a packaging design issue. A perforated package has the potential to cause a soft tissue injury to a healthcare
professional handling
372 2020-06-08
2018-05-07 Class II Package design/selection The needle associated with certain suture product codes has the potential to perforate the packaging due to a packaging design issue. A perforated package has the potential to cause a soft tissue injury to a healthcare
professional handling
4452 2020-06-08

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
P890002 1989-05-31 POLYPROPYLENE SURGICAL SUTURE Alcon Laboratories, Inc.
P820083 1986-08-05 GORE-TEX(R) EXPANDED PTFE SUTURE W. L. Gore & Associates, 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