Adira

ADIRA Plate, 1-Hole, 10.5mm, Static

Registry build 21.09.26
3manufacturers in China registered for this device type
11catalogue numbers in this listing
11510(k) clearances naming this product code

Who Else Makes It

Concentrated in Shandong (2), Jiangsu (1). 2 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code OVD
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
Medtronic (Changzhou) Medical Devices Technology Co., Ltd. Changzhou Jiangsu Manufacturer 53

Record

Regulatory record for Adira
Listed by Globus Medical, Inc., United States
FDA product code OVD
Device type Intervertebral Fusion Device With Integrated Fixation, Lumbar
Device class Class 2
Regulation 21 CFR 888.3080
Establishment Manufacturer, Exporter
510(k) K233735
Record published 2024-04-01
Record revised 2025-11-20 (version 2)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Sterilisation Moist Heat or Steam Sterilization
Single use Yes
Label carries lot or batch number

Catalogue Numbers

Catalogue numbers for Adira
Catalogue number Size Status
1264.1010 In distribution
1264.0004 In distribution
6264.0200 In distribution
1264.0101 In distribution
1264.1009 In distribution
1264.2015 In distribution
1264.1008 In distribution
1264.0001 In distribution
1264.2017 In distribution
1264.2119 In distribution
1264.2117 In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Sirion Astura Medical 1,465
IdentiTi Alphatec Spine, Inc. 1,372
EL Capitan Astura Medical 1,205
Zavation Zavation 1,157
Brigade Nuvasive, Inc. 1,005
Solar™ Interbody Fusion System Degen Medical 899
Zavation F3D Corpectomy Zavation 730
ROI-A Ldr Spine USA 552
Avenue L Ldr Spine USA 524
Transcend Nanotec Alphatec Spine, Inc. 485
Endoskeleton® TL Hyperlordotic nanoLOCK® Surface Technology Titan Spine, LLC 462
Base Nuvasive, Inc. 462

Showing 12 of 241. All products under Intervertebral Fusion Device With Integrated Fixation, Lumbar

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K253401 2026-04-29
K201087 2020-07-31
K170157 2017-09-25
K161379 2016-09-29
K160597 2016-08-29
K161223 2016-07-15
K142498 2015-02-26
K132559 2013-12-30
K120101 2012-03-27
K103382 2011-05-20
K082252 2008-11-05

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