DemeDAC

Polyester Multifilament,Uncoated, Sterile, Nonabsorbable Suture

Registry build 21.09.26
6manufacturers in China registered for this device type
39catalogue numbers in this listing
2510(k) clearances naming this product code

Who Else Makes It

Concentrated in Shanghai (2), Shandong (2), Fujian (1).

Chinese manufacturers registered for FDA product code GAT
Manufacturer City Province Registered as Device types
Zimmer (Shanghai) Medical International Trading Co., Ltd. Shanghai Shanghai Exporter 106
Arthrex (Shanghai) Co., Ltd. Shanghai Shanghai Exporter 38
Shandong Haidike Medical Products Co., Ltd. Heze Shandong Manufacturer 22
Xiamen Zhiyuan Medical Technology Co., Ltd. Xiamen Fujian Contract 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 DemeDAC
Listed by Demetech Corp., United States
FDA product code GAT
Device type Suture, Nonabsorbable, Synthetic, Polyethylene
Device class Class 2
Regulation 21 CFR 878.5000
Establishment Contract manufacturer, Complaint-file establishment, Manufacturer
510(k) K023030
Record published 2019-07-11
Record revised 2026-04-13 (version 4)

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 25 °C
Packaging Pack of 12

Catalogue Numbers

Catalogue numbers for DemeDAC
Catalogue number Size Status
PT156011F13M In distribution
PT144013F4P In distribution
PT15400,8C9P In distribution
PT244548B0T In distribution
PT152026F4P In distribution
PT840050AX20P In distribution
PT14500,8E9P In distribution
PT150548C0P In distribution
PT850536B1P In distribution
PT240036B0P In distribution
PT850548C0P In distribution
PT85565C23T In distribution
PT15500,8E9P In distribution
PT155013F13M In distribution
PT240175G4P In distribution
PT850565C16P In distribution
PT15400,8E9P In distribution
PT243026B0P In distribution
PT154019F4P In distribution
PT14600,8E9P In distribution
PT242026B0P In distribution
PT250340B4P In distribution
PT2455 In distribution
PT840045AX20P In distribution
PT153024F4P In distribution
PT240645C16P In distribution
PT2X11403 In distribution
PT154013F13M In distribution
PT85565C16T In distribution
PT95565C16T In distribution
PT8x140036B0P In distribution
PT945013F13M In distribution
PT850580C16P In distribution
PT944013F13M In distribution
PT250140B4P In distribution
PT6X1401 In distribution
PT245548C1T In distribution
PT15600,8E9P In distribution
PT254013F13M In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Premicron B Braun Surgical SA 1,377
Deknatel Teleflex Medical LLC 1,198
FlexiGRAFT® LifeNet Health 992
DemeBOND Demetech Corp. 939
Ti-Cron Covidien LP 482
HS FIber Riverpoint Medical LLC 413
Ethibond Excel Ethicon, Inc. 383
Arthrex® Arthrex, Inc. 307
Dagrofil B Braun Surgical SA 195
WEGO-Polyester Nonabsorbable Surgical Suture With Needle Foosin Medical Supplies Inc.ltd 175
Cardioxyl ® Peters Surgical 162
Silkam B Braun Surgical SA 150

Showing 12 of 275. All products under Suture, Nonabsorbable, Synthetic, Polyethylene

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K190777 2019-07-31
K023030 2003-06-18

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
N16374 1986-01-23 PROLENE*POLYPROPYLENE SUTURE NONABSORBABLE SURG. S Ethicon, Inc.
P810028 1984-12-17 DEKLENE(TM) Deknatel, Inc.
N17825 1981-09-24 SURGILENE 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