Deploy™ Expandable Interbody System

Deploy is a lumbar interbody fusion implant designed for insertion followed by rotation inside the disc space. A deployed arm forms the bone-graft containment region. The titanium-alloy…

Registry build 21.09.26

Deploy is a lumbar interbody fusion implant designed for insertion followed by rotation inside the disc space. A deployed arm forms the bone-graft containment region.

The titanium-alloy implant has ridges on its upper and lower surfaces to engage the endplates and resist expulsion. Different shapes and heights accommodate the treated anatomy.

Listed Item

Lumbar Expandable Cage, 16 Degree, 28mm Length, 16mm Height

System Components

The system includes trial instruments for size selection, placement instruments and sterilization trays. Implants and stainless-steel instruments are supplied nonsterile for preparation before use. Autograft and/or allogeneic graft and supplemental lumbosacral fixation are required.

14manufacturers in China registered for this device type
80catalogue numbers in this listing
1510(k) clearance

Who Else Makes It

Concentrated in Jiangsu (6), Shandong (2), Shanghai (2). 7 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code MAX
Manufacturer City Province Registered as Device types
Apex (Guangzhou) Tools & Orthopedics Company Guangzhou Guangdong Contract manufacturer 62
Paragon Medical Device (Changzhou) Co., Ltd. Changzhou Jiangsu Contract manufacturer 53
Shandong Weigao Orthopaedic Device Co., Ltd. Weihai Shandong Contract manufacturer 42
Suzhou Ahno Medical Devices Co., Ltd. Suzhou Jiangsu Contract manufacturer 17
Zibo Dante Co., Ltd. Zibo Shandong Contract manufacturer 17
Jiangsu Ideal Medical Science & Technology Co., Ltd. Zhangjiagang Jiangsu Contract manufacturer 7
Zhisu Health Tech Jiaxing Co., Ltd. Tongxiang Zhejiang Contract manufacturer 4
Medtronic (Changzhou) Medical Devices Technology Co., Ltd. Changzhou Jiangsu Manufacturer 53
Shanghai Reach Medical Instrument Co., Ltd. Shanghai Shanghai Manufacturer 30
Changzhou Geasure Medical Apparatus AND Instruments Co., Ltd. Changzhou Jiangsu Contract manufacturer 25
Double Medical Technology Inc. Xiamen Fujian Contract manufacturer 14
Zhejiang Decans Medical Devices Co., Ltd. Jiaxing Zhejiang Manufacturer 10

Showing 12 of 14. All 14 manufacturers in China registered for Intervertebral Fusion Device With Bone Graft, Lumbar

Record

Regulatory record for Deploy™ Expandable Interbody System
Listed by Southern Spine, LLC, United States
FDA product code MAX
Device type Intervertebral Fusion Device With Bone Graft, Lumbar
Device class Class 2
Regulation 21 CFR 888.3080
Establishment Specification developer, Manufacturer
510(k) K211845
Record published 2022-01-10
Record revised 2026-02-09 (version 3)

Specifications

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

Catalogue Numbers

Catalogue numbers for Deploy™ Expandable Interbody System
Catalogue number Size Status
D-001232 In distribution
D-081528 In distribution
D-081328 In distribution
TR-0x16 In distribution
BT-1243 In distribution
D-081432 In distribution
TR-8×17 In distribution
D-001728 In distribution
D-000932 In distribution
D-161628 In distribution
TR-0x11 In distribution
D-001432 In distribution
D-081028 In distribution
D-001528 In distribution
RA-1343 In distribution
D-000832 In distribution
D-081332 In distribution
D-081032 In distribution
C-1359 In distribution
TR-8×12 In distribution
BT-1246 In distribution
TR-0x8 In distribution
D-001428 In distribution
D-001732 In distribution
DT-1245 In distribution
TR-0x17 In distribution
D-081132 In distribution
D-001028 In distribution
D-081228 In distribution
D-000828 In distribution
D-161328 In distribution
D-081628 In distribution
D-081428 In distribution
TR-8×15 In distribution
D-001632 In distribution
DT-1227 In distribution
TR-8×11 In distribution
D-081232 In distribution
DT-1233 In distribution
D-081128 In distribution
D-001328 In distribution
TR-16X15 In distribution
TR-16X14 In distribution
D-001128 In distribution
DT-1230 In distribution
D-001532 In distribution
D-000928 In distribution
C-1360 In distribution
D-001132 In distribution
TR-0x13 In distribution
TR-0x14 In distribution
TR-0x9 In distribution
TY-1350 In distribution
D-161428 In distribution
TR-0x10 In distribution
TR-8×10 In distribution
D-001228 In distribution
DT-1244 In distribution
D-161528 In distribution
D-001332 In distribution
D-001628 In distribution
TR-8×16 In distribution
TR-0x15 In distribution
TR-0x12 In distribution
TR-8×13 In distribution
D-161728 In distribution
TR-16X16 In distribution
D-081632 In distribution
D-081728 In distribution
D-081732 In distribution
TR-16X13 In distribution
D-001032 In distribution
TY-1351 In distribution
TR-16X17 In distribution
D-081532 In distribution
C-1361 In distribution
RA-1341 In distribution
AC-1345 In distribution
BT-1239 In distribution
TR-8×14 In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Peridot Intervertebral body fusion system Gbs Commonwealth Co., Ltd. 10,850
Yellowstone Summit Spine 6,654
CoRoent Nuvasive, Inc. 5,690
Zavation Zavation 2,554
Anyplus II Spinal Fixation System GS Medical Co., Ltd. 2,533
Talos® IBF Meditech Spine, LLC 2,163
Peridot-PT Intervertebral body fusion system Gbs Commonwealth Co., Ltd. 1,956
TirboLOX-L Lumbar Ibfd Captiva Spine, Inc. 1,926
Endoskeleton® TL Titan Spine, LLC 1,896
Evos Lumbar Interbody System Cutting Edge Spine 1,871
Epiphany Pantheon Spinal LLC 1,507
LnK Lumbar Interbody Fusion Cage System L&K Biomed Co., Ltd. 1,506

Showing 12 of 1,958. All products under Intervertebral Fusion Device With Bone Graft, Lumbar

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K211845 2021-11-16

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
P000028 2004-06-18 AFFINITY ANTERIOR CERVICAL CAGE SYSTEM Medtronic Sofamor Danek USA, Inc.
P970015 2003-09-10 LT-CAGE PEEK LUMBAR TAPERED FUSION DEVICE Sofamor Danek
P980048 2001-04-20 BAK/CERVICAL (BAK/C) INTERBODY FUSION SYSTEM Sulzer Spine-Tech
P950019 1999-03-19 RAY THREADED FUSION CAGE (TFC) DEVICE WITH INSTRUMENTATION Stryker Spine
P950002 1997-06-30 BAK INTERBODY FUSION SYSTEM Zimmer Spine, 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