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GBS Commonwealth Co., Ltd.

US

Last updated May 23, 2026

What GBS Commonwealth Co., Ltd. makes

GBS Commonwealth Co., Ltd. manufactures spinal fixation devices, including non-sterile bone-screw systems, metallic and polymeric interbody fusion cages, rods, connectors, hooks, and non-bioabsorbable spinal screws and plates. Their portfolio includes systems like The JASPER Spinal Fixation System and the Peridot Intervertebral Body Fusion System, designed for internal spinal stabilization and fusion procedures.

These devices are classified as Class II under FDA regulations and are listed in the FDA’s Unique Device Identification (UDI) system. The company operates from the United States.

Written from this company's registered devices by an AI model, and not verified by a human reviewer.

Frequently asked questions

What types of medical devices does GBS Commonwealth Co., Ltd. manufacture?

GBS Commonwealth Co., Ltd. specializes in spinal fixation devices. Their product portfolio includes non-sterile bone-screw internal spinal fixation systems, metallic and polymeric interbody fusion cages, rods, connectors, hooks, and non-bioabsorbable spinal screws and plates. These devices are primarily used for internal spinal stabilization and fusion procedures, such as The JASPER Spinal Fixation System and the Peridot Intervertebral Body Fusion System.

Where is GBS Commonwealth Co., Ltd. based?

GBS Commonwealth Co., Ltd. is headquartered in the United States. The company’s location is relevant for regulatory oversight and compliance, as it operates under U.S. medical device regulations.

Which regulatory registries list GBS Commonwealth Co., Ltd.’s devices?

GBS Commonwealth Co., Ltd.’s devices are listed in the FDA’s Unique Device Identification (UDI) system. This registry ensures traceability and transparency in the medical device supply chain, allowing for easier tracking of devices like their spinal fixation systems and interbody fusion cages.

How are GBS Commonwealth Co., Ltd.’s devices classified under FDA regulations?

GBS Commonwealth Co., Ltd.’s devices fall under Class II classification according to FDA regulations. This classification applies to devices that generally pose moderate risk and require special controls to ensure their safety and effectiveness, such as spinal fixation systems and interbody fusion cages.

AI-generated from registry data and not verified by a human reviewer.

Information

Country
US
Address
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Website
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LinkedIn
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Facebook
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Email
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Phone
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PRRC Contact
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EUDAMED SRN
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FDA FEI Number
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DUNS Number
694609156

Catalogue (50209)

Page 14 of 500
DeviceModel / ReferenceRegistriesClassStatus
The JASPER Spinal Fixation System L11D-6035
FDA UDI
Class IIActive
The JASPER Spinal Fixation System L116-7550
FDA UDI
Class IIActive
Peridot Intervertebral body fusion system L361-4457
FDA UDI
Class IIActive
Peridot Intervertebral body fusion system L362-D4B5
FDA UDI
Class IIActive
Peridot Intervertebral body fusion system L361-E858
FDA UDI
Class IIActive
Peridot Intervertebral body fusion system L361-42A2
FDA UDI
Class IIActive
Peridot Intervertebral body fusion system L351-A847
FDA UDI
Class IIActive
Peridot Intervertebral body fusion system L351-604B
FDA UDI
Class IIActive
The JASPER Spinal Fixation System L24E-9095
FDA UDI
Class IIActive
The JASPER Spinal Fixation System L249-5555
FDA UDI
Class IIActive
The JASPER Spinal Fixation System L23G-0545
FDA UDI
Class IIActive
The JASPER Spinal Fixation System L224-0595
FDA UDI
Class IIActive
The JASPER Spinal Fixation System L155-60135
FDA UDI
Class IIActive
Peridot Intervertebral body fusion system L323-00A2
FDA UDI
Class IIActive
The JASPER Spinal Fixation System L154-60160
FDA UDI
Class IIActive
The JASPER Spinal Fixation System L132-0004
FDA UDI
Class IIActive
The JASPER Spinal Fixation System L11G-65150
FDA UDI
Class IIActive
Peridot Intervertebral body fusion system L351-8448
FDA UDI
Class IIActive
The JASPER Spinal Fixation System L11G-8030
FDA UDI
Class IIActive
The JASPER Spinal Fixation System L11C-80110
FDA UDI
Class IIActive
Peridot Intervertebral body fusion system L361-04CB
FDA UDI
Class IIActive
The JASPER Spinal Fixation System L24H-70105
FDA UDI
Class IIActive
The JASPER Spinal Fixation System L22H-8575
FDA UDI
Class IIActive
The JASPER Spinal Fixation System L114-8530
FDA UDI
Class IIActive
Peridot Intervertebral body fusion system L361-424B
FDA UDI
Class IIActive
Peridot Intervertebral body fusion system L351-C8B8
FDA UDI
Class IIActive
Peridot Intervertebral body fusion system L351-08A9
FDA UDI
Class IIActive
Peridot Intervertebral body fusion system L343-E82J
FDA UDI
Class IIActive
Peridot Intervertebral body fusion system L343-E575
FDA UDI
Class IIActive
The JASPER Spinal Fixation System L23M-7050
FDA UDI
Class IIActive
The JASPER Spinal Fixation System L174-166S
FDA UDI
Class IIActive
The JASPER Spinal Fixation System L216-8080
FDA UDI
Class IIActive
The JASPER Spinal Fixation System L154-55360
FDA UDI
Class IIActive
Peridot Intervertebral body fusion system L332-80BC
FDA UDI
Class IIActive
Peridot Intervertebral body fusion system L332-00B4
FDA UDI
Class IIActive
The JASPER Spinal Fixation System L187-5150
FDA UDI
Class IIActive
The JASPER Spinal Fixation System L183-5145
FDA UDI
Class IIActive
The JASPER Spinal Fixation System L238-7035
FDA UDI
Class IIActive
The JASPER Spinal Fixation System L121-2831
FDA UDI
Class IIActive
The JASPER Spinal Fixation System L11B-70120
FDA UDI
Class IIActive
The JASPER Spinal Fixation System L117-80115
FDA UDI
Class IIActive
The JASPER Spinal Fixation System L116-7055
FDA UDI
Class IIActive
The JASPER Spinal Fixation System L22N-05105
FDA UDI
Class IIActive
Peridot Anterior Cervical Intervertebral Body Fusion System C22F-1413
FDA UDI
Class IIActive
The JASPER Spinal Fixation System L11B-8555
FDA UDI
Class IIActive
The JASPER Spinal Fixation System L117-75145
FDA UDI
Class IIActive
The JASPER Spinal Fixation System L117-5560
FDA UDI
Class IIActive
The JASPER Spinal Fixation System L114-65145
FDA UDI
Class IIActive
Peridot-PT Intervertebral body fusion system L628-0022S
FDA UDI
Class IIActive
The JASPER Spinal Fixation System L118-65100
FDA UDI
Class IIActive

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