WaveForm ™ C

Interbody, 16x14x11mm, 10 Degree, 3D

Registry build 21.09.26
7manufacturers in China registered for this device type
34catalogue numbers in this listing
4510(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 WaveForm ™ C
Listed by Seaspine Orthopedics Corporation, 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, Complaint-file establishment, Manufacturer
510(k) K201073
Record published 2020-10-19
Record revised 2025-10-24 (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

Catalogue Numbers

Catalogue numbers for WaveForm ™ C
Catalogue number Size Status
AC1-285127 In distribution
AC1-225081 In distribution
AC1-264111 In distribution
AC1-225091 In distribution
AC1-285117 In distribution
AC1-243087 In distribution
AC1-285111 In distribution
AC1-225101 In distribution
AC1-243071 In distribution
AC1-264087 In distribution
AC1-285081 In distribution
AC1-243127 In distribution
AC1-264127 In distribution
AC1-225107 In distribution
AC1-264071 In distribution
AC1-264067 In distribution
AC1-264057 In distribution
AC1-225067 In distribution
AC1-243091 In distribution
AC1-285077 In distribution
AC1-243107 In distribution
AC1-264117 In distribution
AC1-264121 In distribution
AC1-243077 In distribution
AC1-225087 In distribution
AC1-225071 In distribution
AC1-264077 In distribution
AC1-285071 In distribution
AC1-285061 In distribution
AC1-243117 In distribution
AC1-243101 In distribution
AC1-243057 In distribution
AC1-225121 In distribution
AC1-225057 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
K220296 2023-02-03
K183083 2019-02-14
K172926 2017-12-21
K171046 2017-07-07

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