Lupine Orthocord

LUPINE BR Anchor W/DS ORTHOCORD TCP/PLGA Absorbable Anchor, with dual size 2 (5 metric) braided composite suture, violet and blue, 36 Inches (91cm). Size 2 (5 metric) eyelet loop.

Registry build 21.09.26
6manufacturers in China registered for this device type
1catalogue number

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 Lupine Orthocord
Listed by Medos International Sàrl, Switzerland
FDA product code GAT
Device type Suture, Nonabsorbable, Synthetic, Polyethylene
Device class Class 2
Regulation 21 CFR 878.5000
510(k) K040827
Record published 2015-09-01
Record revised 2025-04-11 (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

Catalogue Numbers

Catalogue numbers for Lupine Orthocord
Catalogue number Size Status
210712 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

Recalls Naming This Product

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

Recalls naming the identifiers of Lupine Orthocord
Recalled by Identified by Initiated FDA class Root cause Reason Quantity Closed
DePuy Mitek, Inc. 510(k) number 2023-04-13 Class II Use error IFU Warning: Applying bending force and/or bending force with impaction to the BIOKNOTLESS Anchor Inserter may cause a fragment of the inserter tip to break off during use and be retained in the patient. broken BIOKNOTLESS Anchor inserter t 805 units
DePuy Mitek, Inc. 510(k) number 2023-04-13 Class II Use error IFU Warning: Applying bending force and/or bending force with impaction to the BIOKNOTLESS Anchor Inserter may cause a fragment of the inserter tip to break off during use and be retained in the patient. broken BIOKNOTLESS Anchor inserter t 540 units
DePuy Mitek, Inc. 510(k) number 2023-04-13 Class II Use error IFU Warning: Applying bending force and/or bending force with impaction to the BIOKNOTLESS Anchor Inserter may cause a fragment of the inserter tip to break off during use and be retained in the patient. broken BIOKNOTLESS Anchor inserter t 2372 units
DePuy Mitek, Inc. 510(k) number 2023-04-13 Class II Use error IFU Warning: Applying bending force and/or bending force with impaction to the BIOKNOTLESS Anchor Inserter may cause a fragment of the inserter tip to break off during use and be retained in the patient. broken BIOKNOTLESS Anchor inserter t 3328 units
DePuy Mitek, Inc. 510(k) number 2023-04-13 Class II Use error IFU Warning: Applying bending force and/or bending force with impaction to the BIOKNOTLESS Anchor Inserter may cause a fragment of the inserter tip to break off during use and be retained in the patient. broken BIOKNOTLESS Anchor inserter t 1125 units
DePuy Mitek, Inc. 510(k) number 2012-01-27 Not classified Process control Lupine BR Anchor w/ Orthocord may be assembled with an incorrect suture configuration and result in a loose repair 41581 2015-08-05
DePuy Mitek, Inc. 510(k) number 2012-01-27 Not classified Process control Lupine BR Anchor w/ Orthocord may be assembled with an incorrect suture configuration and result in a loose repair 1243 units 2015-08-05
DePuy Mitek, Inc. 510(k) number 2012-01-27 Not classified Process control Lupine BR Anchor w/ Orthocord may be assembled with an incorrect suture configuration and result in a loose repair 1757 units 2015-08-05
DePuy Mitek, Inc. 510(k) number 2012-01-27 Not classified Process control Lupine BR Anchor w/ Orthocord may be assembled with an incorrect suture configuration and result in a loose repair 32408 units 2015-08-05
DePuy Mitek, Inc. 510(k) number 2012-01-27 Not classified Process control Lupine BR Anchor w/ Orthocord may be assembled with an incorrect suture configuration and result in a loose repair 24146 units 2015-08-05
DePuy Mitek, Inc. 510(k) number 2012-01-27 Not classified Process control Lupine BR Anchor w/ Orthocord may be assembled with an incorrect suture configuration and result in a loose repair 2015-08-05
DePuy Mitek, Inc. 510(k) number 2012-01-27 Not classified Process control Lupine BR Anchor w/ Orthocord may be assembled with an incorrect suture configuration and result in a loose repair 56468 units 2015-08-05
DePuy Mitek, Inc. 510(k) number 2012-01-27 Not classified Process control Lupine BR Anchor w/ Orthocord may be assembled with an incorrect suture configuration and result in a loose repair 2015-08-05
DePuy Mitek, Inc. 510(k) number 2012-01-27 Not classified Process control Lupine BR Anchor w/ Orthocord may be assembled with an incorrect suture configuration and result in a loose repair 20476 units 2015-08-05
DePuy Mitek, Inc. 510(k) number 2012-01-27 Not classified Process control Lupine BR Anchor w/ Orthocord may be assembled with an incorrect suture configuration and result in a loose repair 12774 2015-08-05
DePuy Mitek, Inc. 510(k) number 2011-10-31 Not classified Employee error Incorrect suture configuration 298 units 2015-08-05
DePuy Mitek, Inc. 510(k) number 2011-10-31 Not classified Employee error Incorrect suture configuration 299 units 2015-08-05
DePuy Mitek, Inc. 510(k) number 2011-10-31 Not classified Employee error Incorrect suture configuration 291 units 2015-08-05
DePuy Mitek, Inc. 510(k) number 2011-10-31 Not classified Employee error Incorrect suture configuration 585 units 2015-08-05
DePuy Mitek, Inc. 510(k) number 2011-10-31 Not classified Employee error Incorrect suture configuration 295 units 2015-08-05
DePuy Mitek, Inc. 510(k) number 2008-04-29 Not classified Employee error Lupine BR Anchor w/Orthocord was assembled with an incorrect suture configuration. The suture loop was not assembled at the distal end of the anchor. It was only threaded through the suture hole in the anchor. Risk associated with incorr 105 units 2008-10-02

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