Modulus

Modulus-C Trial, 6x17x14mm 10° Hard Stop

Registry build 21.09.26
7manufacturers in China registered for this device type
91catalogue numbers in this listing
3510(k) clearances naming this product code

Who Else Makes It

Concentrated in Shanghai (2), Shandong (2), Zhejiang (2). 3 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code ODP
Manufacturer City Province Registered as Device types
Shandong Weigao Orthopaedic Device Co., Ltd. Weihai Shandong Contract manufacturer 42
Zibo Dante Co., Ltd. Zibo Shandong Contract manufacturer 17
Zhisu Health Tech Jiaxing Co., Ltd. Tongxiang Zhejiang Contract manufacturer 4
Zimmer (Shanghai) Medical International Trading Co., Ltd. Shanghai Shanghai Exporter 106
Medtronic (Changzhou) Medical Devices Technology Co., Ltd. Changzhou Jiangsu Manufacturer 53
Zhejiang Decans Medical Devices Co., Ltd. Jiaxing Zhejiang Manufacturer 10
Shanghai Sanyou Medical Co., Ltd. Shanghai Shanghai Manufacturer 6

Record

Regulatory record for Modulus
Listed by Nuvasive, Inc., United States
FDA product code ODP
Device type Intervertebral Fusion Device With Bone Graft, Cervical
Device class Class 2
Regulation 21 CFR 888.3080
Establishment Specification developer, Repacker / relabeller, Complaint-file establishment, Manufacturer, Exporter
510(k) K172676
Record published 2019-02-12
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 Modulus
Catalogue number Size Status
67940038P2 In distribution
67940082P2 In distribution
67940072P2 In distribution
6793049P2 In distribution
67950047 In distribution
67950037 In distribution
6793039P2 In distribution
67950038 In distribution
6793072P2 In distribution
67940071P2 In distribution
67950017 In distribution
6793144 In distribution
6793038P2 In distribution
67950014 In distribution
67940017P2 In distribution
6793037P2 In distribution
67950084 In distribution
67950083 In distribution
67940051P2 In distribution
67940012P2 In distribution
67950036 In distribution
67950002 In distribution
67950016 In distribution
6793047P2 In distribution
67950051 In distribution
67950070 In distribution
67940016P2 In distribution
67950040 In distribution
67940014P2 In distribution
67950049 In distribution
6793071P2 In distribution
6793048P2 In distribution
67950013 In distribution
67940050P2 In distribution
67940069P2 In distribution
67940000P2 In distribution
67940013P2 In distribution
6793015P2 In distribution
67940005P2 In distribution
6793050P2 In distribution
67940040P2 In distribution
6793002P2 In distribution
67940084P2 In distribution
67950035 In distribution
6793014P2 In distribution
6793004P2 In distribution
67950072 In distribution
67950003 In distribution
67950080 In distribution
67950039 In distribution
67950071 In distribution
67940003P2 In distribution
6793146 In distribution
67940068P2 In distribution
67940002P2 In distribution
67940035P2 In distribution
67950015 In distribution
67950082 In distribution
67940073P2 In distribution
6793016P2 In distribution
6793001P2 In distribution
67950068 In distribution
67950000 In distribution
67940047P2 In distribution
67940039P2 In distribution
67940070P2 In distribution
67940037P2 In distribution
67950050 In distribution
67940081P2 In distribution
67940048P2 In distribution
67940049P2 In distribution
6793013P2 In distribution
6793003P2 In distribution
67950069 In distribution
67950004 In distribution
67950005 In distribution
6793070P2 In distribution
67940080P2 In distribution
67950081 In distribution
67940083P2 In distribution
6793147 In distribution
67950048 In distribution
67950073 In distribution
67940001P2 In distribution
67950001 In distribution
67940036P2 In distribution
67940015P2 In distribution
6793036P2 In distribution
67950012 In distribution
6793145 In distribution
67940004P2 In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Latitude-C AM™ Cervical Interbody Fusion System Degen Medical 1,529
IdentiTi Alphatec Spine, Inc. 1,390
Zavation Zavation 1,357
IVA Cage Ti Diomedical Co., Ltd. 1,202
Latitude-C Cervical Interbody Spacer System Degen Medical 1,185
Peridot Anterior Cervical Intervertebral Body Fusion System Gbs Commonwealth Co., Ltd. 1,056
Aleutian® Interbody Systems VB Spine LLC 1,017
Valeo Spacer System Sintx Technologies Inc. 918
Cascadia™ Interbody System VB Spine LLC 823
CoRoent Nuvasive, Inc. 815
Tyber Medical Tyber Medical 740
Matisse Anterior Cervical Interbody Fusion Cage System CTL Medical Corporation 577

Showing 12 of 938. All products under Intervertebral Fusion Device With Bone Graft, Cervical

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K223731 2023-01-12
K140003 2014-04-03
K081611 2008-10-02

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