Cohere

COHERE TLIF-O Inserter, 10mm Impaction

Registry build 21.09.26
1manufacturer
69catalogue numbers in this listing

Who Else Makes It

Registered in Shandong. One is registered as a contract manufacturer, able to build to a specification.

Chinese manufacturers registered for FDA product code PHM
Manufacturer City Province Registered as Device types
Shandong Weigao Orthopaedic Device Co., Ltd. Weihai Shandong Contract manufacturer 42

Record

Regulatory record for Cohere
Listed by Nuvasive, Inc., United States
FDA product code PHM
Device type Intervertebral Fusion Device With Bone Graft, Thoracic
Device class Class 2
Regulation 21 CFR 888.3080
Establishment Specification developer, Repacker / relabeller, Complaint-file establishment, Manufacturer, Exporter
510(k) K181860
Record published 2020-11-16
Record revised 2025-06-11 (version 5)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Sterilisation Radiation Sterilization
Supplied sterile Yes
Single use Yes
Prescription Prescription only
Label carries lot or batch number, expiry date, manufacturing date

Catalogue Numbers

Catalogue numbers for Cohere
Catalogue number Size Status
4119305P2 In distribution
6160302P2 In distribution
6140258P2 In distribution
6124304P2 In distribution
8267255P2 In distribution
8150855P2 In distribution
D1814390 In distribution
D1814377 In distribution
8227255P2 In distribution
8227160P2 In distribution
8227245P2 In distribution
8106015P2 In distribution
8126015P2 In distribution
8227145P2 In distribution
4151345P2 In distribution
8267260P2 In distribution
8105015P2 In distribution
D1814394 In distribution
4144348P2 In distribution
8267855P2 In distribution
6144304P2 In distribution
4121308P2 In distribution
8267850P2 In distribution
4141305P2 In distribution
8187145P2 In distribution
6140304P2 In distribution
6160258P2 In distribution
8187860P2 In distribution
8221250P2 In distribution
8125515P2 In distribution
8227860P2 In distribution
4129305P2 In distribution
8187260P2 In distribution
D1814386 In distribution
6120308P2 In distribution
8261260P2 In distribution
1814379 In distribution
4124348P2 In distribution
8187160P2 In distribution
6140302P2 In distribution
6160254P2 In distribution
4121348P2 In distribution
4151305P2 In distribution
8267860P2 In distribution
1814364 In distribution
8221260P2 In distribution
6160304P2 In distribution
8267245P2 In distribution
8150860P2 In distribution
8187155P2 In distribution
8180850P2 In distribution
6180252P2 In distribution
8260850P2 In distribution
8267250P2 In distribution
8220855P2 In distribution
8261255P2 In distribution
4119308P2 In distribution
8104515P2 In distribution
4144308P2 In distribution
6180302P2 In distribution
4131345P2 In distribution
6120258P2 In distribution
8221055P2 In distribution
4129308P2 In distribution
6110308P2 In distribution
8181250P2 In distribution
6180308P2 In distribution
6140354P2 In distribution
8220860P2 In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
CoRoent Nuvasive, Inc. 2,299
IdentiTi Alphatec Spine, Inc. 940
Solar™ Interbody Fusion System Degen Medical 805
Transcend Nanotec Alphatec Spine, Inc. 466
IDENTITi Nanotec Alphatec Spine, Inc. 459
E3D-A Interbody System Evolution Spine, LLC 308
Battalion Alphatec Spine, Inc. 241
Reef L Seaspine Orthopedics Corporation 207
IdentiTi II Alphatec Spine, Inc. 163
Modulus Nuvasive, Inc. 158
Hedron Globus Medical, Inc. 156
Roccia Silony Medical Gmbh 133

Showing 12 of 41. All products under Intervertebral Fusion Device With Bone Graft, Thoracic

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