Vu Apod™ – L

LATERAL IMPLANT, STANDARD SPINPLATE™, LORDOTIC, 10mm X 60mm X 10°

Registry build 21.09.26
14manufacturers in China registered for this device type
120catalogue numbers in this listing
20510(k) clearances naming this product code
1recall

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 Vu aPod™ – L
Listed by Seaspine Orthopedics Corporation, 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, Complaint-file establishment, Manufacturer
510(k) K112986
Record published 2015-09-24
Record revised 2025-10-24 (version 6)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Sterilisation Moist Heat or Steam Sterilization
Prescription Prescription only
Label carries lot or batch number
Distribution end date 2016-09-02

Catalogue Numbers

Catalogue numbers for Vu aPod™ – L
Catalogue number Size Status
31-29-1245 12mm X 18mm X 45mm In distribution
31-24-1660-12 LORDOTIC, 16mm X 23mm X 60mm X 12° In distribution
31-25-1245-12 12mm X 23mm X 45mm X 12° In distribution
31-14-1260-12 12mmx 60mm x 12° In distribution
31-24-1645-12 16mm X 23mm X 45mm X 12° In distribution
31-20-0840 8mm x 23mm x 40mm In distribution
31-25-1655-12 16mm X 23mm X 55mm X 12° In distribution
31-24-1650-12 16mm X 23mm X 50mm X 12° In distribution
31-30-0840 8mm X 18mm X 40mm In distribution
31-20-1245 12mm x 23mm x 45mm In distribution
31-29-1055 10mm X 18mm X 55mm In distribution
31-22-1050 10mm x 23mm x 50mm In distribution
31-30-0860 8mm X 18mm X 60mm In distribution
31-10-1040 10mm x 40mm In distribution
31-37-0855-10 8mm X 23mm X 55mm X 10° In distribution
31-30-0850 8mm X 18mm X 50mm In distribution
31-22-1655 16mm x 23mm x 55mm In distribution
31-23-1060-10 10mm x 23mm x 60mm x 10° In distribution
31-31-1050-10 10mm X 18mm X 50mm X 10° In distribution
31-30-1240 12mm X 18mm X 40mm In distribution
31-60-0840-10 8mm X 18mm X 40mm X 10° In distribution
31-22-0845 8mm x 23mm x 45mm In distribution
31-29-1650 16mm X 18mm X 50mm In distribution
31-29-1045 10mm X 18mm X 45mm In distribution
31-20-1250 12mm x 23mm x 50mm In distribution
31-31-1250-12 12mm X 18mm X 50mm X 12° In distribution
31-21-1450 14mm x 23mm x 50mm In distribution
31-13-1255 12mm x 55mm In distribution
31-14-1245-12 12mmx 45mm x 12° In distribution
31-25-1045-10 10mm X 23mm X 45mm X 10° In distribution
31-30-1245 12mm X 18mm X 45mm In distribution
31-20-1055 10mm x 23mm x 55mm In distribution
31-60-0850-10 8mm X 18mm X 50mm X 10° In distribution
31-25-0840-10 8mm X 23mm X 40mm X 10° In distribution
31-32-1445-12 14mm X 18mm X 45mm X 12° In distribution
31-22-1045 10mm x 23mm x 45mm In distribution
31-22-1060 10mm x 23mm x 60mm In distribution
31-31-1450-12 14mm X 18mm X 50mm X 12° In distribution
31-22-1260 12mm x 23mm x 60mm In distribution
31-23-1055-10 10mm x 23mm x 55mm x 10° In distribution
31-32-1040-10 10mm X 18mm X 40mm X 10° In distribution
31-32-1255-12 12mm X 18mm X 55mm X 12° In distribution
31-30-1455 14mm X 18mm X 55mm In distribution
31-22-1455 14mm x 23mm x 55mm In distribution
31-30-1045 10mm X 18mm X 45mm In distribution
31-23-1040-10 10mm x 23mm x 40mm x 10° In distribution
31-22-0855 8mm x 23mm x 55mm In distribution
31-29-1255 12mm X 18mm X 55mm In distribution
31-29-1455 14mm X 18mm X 55mm In distribution
31-22-1255 12mm x 23mm x 55mm In distribution
31-29-1655 16mm X 18mm X 55mm In distribution
31-30-0845 STANDARD, 8mm X 18mm X 45mm In distribution
31-20-1260 12mm x 23mm x 60mm In distribution
31-39-0850-10 8mm X 18mm X 50mm X 10° In distribution
31-25-1255-12 12mm X 23mm X 55mm X 12° In distribution
31-30-1445 14mm X 18mm X 45mm In distribution
31-21-1660 16mm x 23mm x 60mm In distribution
31-29-1640 16mm X 18mm X 40mm In distribution
31-31-1260-12 12mm X 18mm X 60mm X 12° In distribution
31-32-1650-12 16mm X 18mm X 50mm X 12° In distribution
31-13-1250 12mmx 50mm In distribution
31-24-1450-12 14mm X 23mm X 50mm X 12° In distribution
31-21-1455 14mm x 23mm x 55mm In distribution
31-30-1255 12mm X 18mm X 55mm In distribution
31-30-0855 8mm X 18mm X 55mm In distribution
31-14-1240-12 12mmx 40mm x 12° In distribution
31-60-0845-10 8mm X 18mm X 45mm X 10° In distribution
31-29-1460 14mm X 18mm X 60mm In distribution
31-22-1240 12mm x 23mm x 40mm In distribution
31-31-1245-12 12mm X 18mm X 45mm X 12° In distribution
31-32-1660-12 16mm X 18mm X 60mm X 12° In distribution
31-11-1045-10 10mm x 45mm x 10° In distribution
31-30-1660 16mm X 18mm X 60mm In distribution
31-23-1050-10 10mm x 23mm x 50mm x 10° In distribution
31-10-1045 10mm x 45mm In distribution
31-29-1450 14mm X 18mm X 50mm In distribution
31-10-0855 8mm x 55mm In distribution
31-60-0860-10 8mm X 18mm X 60mm X 10° In distribution
31-37-0845-10 8mm X 23mm X 45mm X 10° In distribution
31-22-1645 16mm x 23mm x 45mm In distribution
31-39-0860-10 8mm X 18mm X 60mm X 10° In distribution
31-32-1060-10 10mm X 18mm X 60mm X 10° In distribution
31-22-1450 14mm x 23mm x 50mm In distribution
31-22-1460 14mm x 23mm x 60mm In distribution
31-25-1260-12 12mm X 23mm X 60mm X 12° In distribution
31-32-1050-10 10mm X 18mm X 50mm X 10° In distribution
31-20-1045 10mm x 23mm x 45mm In distribution
31-11-1060-10 10mm x 60mm x 10° In distribution
31-22-0860 8mm x 23mm x 60mm In distribution
31-31-1255-12 12mm X 18mm X 55mm X 12° In distribution
31-31-1440-12 14mm X 18mm X 40mm X 12° In distribution
31-23-1250-12 12mm x 23mm x 50mm x 12° In distribution
31-40-0145 In distribution
31-20-1040 10mm x 23mm x 40mm In distribution
31-29-1250 12mm X 18mm X 50mm In distribution
31-30-1040 10mm X 18mm X 40mm In distribution
31-20-1255 12mm x 23mm x 55mm In distribution
31-39-0845-10 8mm X 18mm X 45mm X 10° In distribution
31-29-1060 10mm X 18mm X 60mm In distribution
31-38-0850-10 8mm X 23mm X 50mm X 10° In distribution
31-30-1650 16mm X 18mm X 50mm In distribution
31-38-0845-10 8mm X 23mm X 45mm X 10° In distribution
31-20-1240 12mm x 23mm x 40mm In distribution
31-32-1245-12 12mm X 18mm X 45mm X 12° In distribution
31-29-1440 14mm X 18mm X 40mm In distribution
31-24-1655-12 16mm X 23mm X 55mm X 12° In distribution
31-25-1040-10 10mm X 23mm X 40mm X 10° In distribution
31-38-0860-10 8mm X 23mm X 60mm X 10° In distribution
31-60-0855-10 8mm X 18mm X 55mm X 10° In distribution
31-38-0855-10 8mm X 23mm X 55mm X 10° In distribution
31-31-1040-10 10mm X 18mm X 40mm X 10° In distribution
31-25-1240-12 12mm X 23mm X 40mm X 12° In distribution
31-30-1645 16mm X 18mm X 45mm In distribution
31-24-1640-12 16mm X 23mm X 40mm X 12° Withdrawn
31-22-1640 16mm x 23mm x 40mm Withdrawn
31-25-1440-12 14mm X 23mm X 40mm X 12° Withdrawn
31-24-1440-12 14mm X 23mm X 40mm X 12° Withdrawn
31-21-1440 14mm x 23mm x 40mm Withdrawn
31-22-1440 14mm x 23mm x 40mm Withdrawn
31-21-1640 16mm x 23mm x 40mm Withdrawn

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
K253420 2026-07-01
K241466 2024-06-20
K240566 2024-04-26
K233694 2024-01-12
K222732 2022-11-07
K220711 2022-05-10
K213420 2022-05-04
K212540 2021-09-10
K210497 2021-07-07
K210583 2021-06-02
K201755 2020-12-15
K201193 2020-11-25
K200879 2020-06-10
K193636 2020-04-24
K193418 2020-03-13
K192132 2019-12-03
K181079 2018-07-18
K173260 2017-12-04
K173022 2017-10-26
K162715 2016-10-28

Recalls

1 of these is Class II. Class II means a temporary or reversible health consequence. Volume alone is not a quality signal: a manufacturer that ships more recalls more.

Recalls referencing this product code
Initiated FDA class Root cause Reason Quantity
2025-08-06 Class II Device Design Inserter, used as part of a system with an intervertebral body fusion device, may contribute to difficulty disengaging the implant or improper implant positioning, which may may lead to prolonged surgery, intraoperative revision, and may r 74

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