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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 24 of 500
DeviceModel / ReferenceRegistriesClassStatus
The JASPER Spinal Fixation System L217-8075
FDA UDI
Class IIActive
The JASPER Spinal Fixation System L215-05115
FDA UDI
Class IIActive
The JASPER Spinal Fixation System L112-95135
FDA UDI
Class IIActive
The JASPER Spinal Fixation System L115-8030
FDA UDI
Class IIActive
The JASPER Spinal Fixation System L115-8050
FDA UDI
Class IIActive
The JASPER Spinal Fixation System L115-6055
FDA UDI
Class IIActive
Peridot Intervertebral body fusion system L351-4446
FDA UDI
Class IIActive
The JASPER Spinal Fixation System L243-6545
FDA UDI
Class IIActive
The JASPER Spinal Fixation System L21H-05120
FDA UDI
Class IIActive
Peridot Intervertebral body fusion system L361-405A
FDA UDI
Class IIActive
Peridot Intervertebral body fusion system L361-A849
FDA UDI
Class IIActive
Peridot Intervertebral body fusion system L361-6041
FDA UDI
Class IIActive
Peridot Intervertebral body fusion system L351-A4B5
FDA UDI
Class IIActive
Peridot Intervertebral body fusion system L343-D906
FDA UDI
Class IIActive
Peridot Intervertebral body fusion system L343-0906
FDA UDI
Class IIActive
The JASPER Spinal Fixation System L24A-8050
FDA UDI
Class IIActive
The JASPER Spinal Fixation System L111-9070
FDA UDI
Class IIActive
Peridot Intervertebral body fusion system L351-84B1
FDA UDI
Class IIActive
Peridot Intervertebral body fusion system L351-E8A3
FDA UDI
Class IIActive
Peridot Intervertebral body fusion system L343-C57B
FDA UDI
Class IIActive
Peridot Intervertebral body fusion system L343-F90H
FDA UDI
Class IIActive
The JASPER Spinal Fixation System L23G-9530
FDA UDI
Class IIActive
The JASPER Spinal Fixation System L114-85120
FDA UDI
Class IIActive
The JASPER Spinal Fixation System L228-9040
FDA UDI
Class IIActive
The JASPER Spinal Fixation System L21G-8530
FDA UDI
Class IIActive
The JASPER Spinal Fixation System L210-0085
FDA UDI
Class IIActive
Peridot Intervertebral body fusion system L351-68B9
FDA UDI
Class IIActive
The JASPER Spinal Fixation System L21F-05110
FDA UDI
Class IIActive
The JASPER Spinal Fixation System L118-70125
FDA UDI
Class IIActive
The JASPER Spinal Fixation System L145-63115
FDA UDI
Class IIActive
The JASPER Spinal Fixation System L144-60185
FDA UDI
Class IIActive
The JASPER Spinal Fixation System L214-7540
FDA UDI
Class IIActive
The JASPER Spinal Fixation System L152-63200
FDA UDI
Class IIActive
The JASPER Spinal Fixation System L144-60125
FDA UDI
Class IIActive
Peridot-PT Intervertebral body fusion system L636-0037S
FDA UDI
Class IIActive
Peridot-PT Intervertebral body fusion system L531-80C8
FDA UDI
Class IIActive
The JASPER Spinal Fixation System L152-63450
FDA UDI
Class IIActive
Peridot Intervertebral body fusion system L362-E8CC
FDA UDI
Class IIActive
The JASPER Spinal Fixation System L22K-0595
FDA UDI
Class IIActive
Peridot Intervertebral body fusion system L331-4193
FDA UDI
Class IIActive
Peridot-PT Intervertebral body fusion system L521-81A2S
FDA UDI
Class IIActive
The JASPER Spinal Fixation System L154-60480
FDA UDI
Class IIActive
Peridot Intervertebral body fusion system L331-00A8
FDA UDI
Class IIActive
Peridot Intervertebral body fusion system L323-0163
FDA UDI
Class IIActive
The JASPER Spinal Fixation System L112-85115
FDA UDI
Class IIActive
Peridot Intervertebral body fusion system L361-84C8
FDA UDI
Class IIActive
Peridot Intervertebral body fusion system L361-B04C
FDA UDI
Class IIActive
The JASPER Spinal Fixation System L113-75120
FDA UDI
Class IIActive
The JASPER Spinal Fixation System L11B-80125
FDA UDI
Class IIActive
The JASPER Spinal Fixation System L141-63310
FDA UDI
Class IIActive

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