Zeus-P

Zeus-P Interbody, 25L x 13W x 16H mm, 5.7 Degree Lordosis

Registry build 21.09.26
14manufacturers in China registered for this device type
163catalogue numbers in this listing
17510(k) clearances naming this product code
2recalls on this code

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 Zeus-P
Listed by Spinal Elements, Inc., 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
Record published 2021-01-09
Record revised 2022-11-08 (version 5)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Sterilisation Moist Heat or Steam Sterilization
Supplied sterile Yes
Single use Yes
Prescription Prescription only
Label carries lot or batch number, expiry date, manufacturing date
Distribution end date 2022-11-08
UDI direct marking Exempt

Catalogue Numbers

Catalogue numbers for Zeus-P
Catalogue number Size Status
105-65-320909 In distribution
105-65-260911 In distribution
1-110926B In distribution
65-300908 In distribution
65-300911 In distribution
PL261314 In distribution
105-65-320910 In distribution
1-140922B In distribution
1-140926B In distribution
1-170926B In distribution
1-160922B In distribution
105-65-320911 In distribution
65-220907 In distribution
PL261311 In distribution
105-65-320915 In distribution
65-220914 In distribution
105-65-320913 In distribution
1-070922B In distribution
PL261312 In distribution
65-300909 In distribution
105-65-260912 In distribution
105-65-320914 In distribution
1-170922B In distribution
65-300915 In distribution
1-150926B In distribution
1-120926B In distribution
105-65-220913 In distribution
65-220917 In distribution
1-180922B In distribution
PL261310 In distribution
65-260917 In distribution
65-300916 In distribution
65-260915 In distribution
65-320918 In distribution
1-130922B In distribution
65-260911 In distribution
1-120922B In distribution
65-300918 In distribution
1-100922B In distribution
105-65-260914 In distribution
65-220918 In distribution
65-300912 In distribution
105-65-320912 In distribution
1-150922B In distribution
65-220908 In distribution
105-65-220912 In distribution
65-260913 In distribution
65-300907 In distribution
105-65-220909 In distribution
65-320907 In distribution
65-320917 In distribution
65-260918 In distribution
1-180926B In distribution
105-65-260907 In distribution
65-300914 In distribution
1-070926B In distribution
1-110922B In distribution
PL261309 In distribution
65-260916 In distribution
65-260908 In distribution
1-090922B In distribution
PL261313 In distribution
1-130926B In distribution
65-220916 In distribution
1-080926B In distribution
105-65-260910 In distribution
65-260909 In distribution
1-080922B In distribution
1-100926B In distribution
PL261315 In distribution
105-65-220915 In distribution
1-090926B In distribution
65-300910 In distribution
65-300917 In distribution
105-65-320908 In distribution
PL261308 In distribution
105-65-220910 In distribution
1-160926B In distribution
65-300913 In distribution
PH251311 Withdrawn
105-65-220914 Withdrawn
PL251314 Withdrawn
105-65-300915 Withdrawn
1001111P Withdrawn
105-65-320917 Withdrawn
1001108BC Withdrawn
1001109BC Withdrawn
PL251311 Withdrawn
1001112BC Withdrawn
1001116P Withdrawn
105-65-260915 Withdrawn
105-65-300917 Withdrawn
105-65-220908 Withdrawn
65-260910 Withdrawn
105-65-300908 Withdrawn
PL251315 Withdrawn
105-65-260918 Withdrawn
65-260907 Withdrawn
PL251309 Withdrawn
105-65-260917 Withdrawn
65-320910 Withdrawn
105-65-300912 Withdrawn
65-320913 Withdrawn
1001114P Withdrawn
65-220912 Withdrawn
65-260912 Withdrawn
1001114BC Withdrawn
105-65-320918 Withdrawn
1001110BC Withdrawn
105-65-300916 Withdrawn
65-320915 Withdrawn
1001111BC Withdrawn
105-65-220917 Withdrawn
65-220911 Withdrawn
PL251308 Withdrawn
PH251308 Withdrawn
1001115P Withdrawn
105-65-300914 Withdrawn
65-320916 Withdrawn
65-320908 Withdrawn
PH251314 Withdrawn
65-320912 Withdrawn
105-65-220907 Withdrawn
105-65-300918 Withdrawn
65-320909 Withdrawn
1001113P Withdrawn
105-65-320907 Withdrawn
105-65-260916 Withdrawn
1001108P Withdrawn
PH251312 Withdrawn
105-65-260909 Withdrawn
PL251310 Withdrawn
65-320914 Withdrawn
PH251315 Withdrawn
PH251310 Withdrawn
105-65-260908 Withdrawn
65-320911 Withdrawn
1001113BC Withdrawn
PL251313 Withdrawn
105-65-300911 Withdrawn
1001115BC Withdrawn
105-65-220918 Withdrawn
65-220910 Withdrawn
65-220909 Withdrawn
105-65-300907 Withdrawn
PL251316 Withdrawn
105-65-220916 Withdrawn
1001112P Withdrawn
105-65-300910 Withdrawn
105-65-300909 Withdrawn
105-65-300913 Withdrawn
PL251312 Withdrawn
105-65-320916 Withdrawn
1001110P Withdrawn
PH251316 Withdrawn
1001109P Withdrawn
65-220915 Withdrawn
105-65-220911 Withdrawn
105-65-260913 Withdrawn
1001107P Withdrawn
PH251309 Withdrawn
65-220913 Withdrawn
PH251313 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
K260506 2026-05-15
K250773 2026-02-04
K234150 2024-03-27
K231252 2023-06-30
K210044 2021-06-30
K203254 2021-03-26
K202298 2020-12-22
K182584 2018-12-10
K181837 2018-11-02
K170235 2017-11-29
K152011 2016-06-09
K150061 2015-05-19
K122967 2013-02-21
K110632 2012-05-23
K081968 2008-08-05
K073348 2007-12-26
K071724 2007-11-09

Recalls

2 of these are 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 Closed
2018-04-16 Class II Labeling mix-ups Omega LIF interbody implants labeled as having 11 degrees of lordosis was assembled using components manufactured with 4 degrees of lordosis. 19 units
2014-12-18 Class II Labeling False and Misleading Spinal Elements is recalling the Ti-Bond related brochures that includes LT-10000 and MP-14000 (all revisions) the content regarding the Ti-Bond coating within the literature is unsubstantiated in context and/or misleading for the coating’s 1200 units 2015-03-10

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