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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 15 of 500
DeviceModel / ReferenceRegistriesClassStatus
The JASPER Spinal Fixation System L114-05145
FDA UDI
Class IIActive
Peridot Intervertebral body fusion system L351-E4C6
FDA UDI
Class IIActive
The JASPER Spinal Fixation System L118-9520
FDA UDI
Class IIActive
The JASPER Spinal Fixation System L115-8520
FDA UDI
Class IIActive
The JASPER Spinal Fixation System L112-90150
FDA UDI
Class IIActive
Peridot Anterior Cervical Intervertebral Body Fusion System C21C-2014
FDA UDI
Class IIActive
Peridot Intervertebral body fusion system L351-E2C8
FDA UDI
Class IIActive
Peridot Intervertebral body fusion system L351-D256
FDA UDI
Class IIActive
The JASPER Spinal Fixation System L23A-7060
FDA UDI
Class IIActive
The JASPER Spinal Fixation System L215-7580
FDA UDI
Class IIActive
The JASPER Spinal Fixation System L221-7040
FDA UDI
Class IIActive
Prase-C Anterior Cervical Plate System C128-4213
FDA UDI
Class IIActive
The JASPER Spinal Fixation System L144-60520
FDA UDI
Class IIActive
The JASPER Spinal Fixation System L144-55360
FDA UDI
Class IIActive
The JASPER Spinal Fixation System L127-2838
FDA UDI
Class IIActive
The JASPER Spinal Fixation System L11F-8590
FDA UDI
Class IIActive
The JASPER Spinal Fixation System L239-6040
FDA UDI
Class IIActive
The JASPER Spinal Fixation System L22D-85100
FDA UDI
Class IIActive
Peridot-TD Intervertebral body fusion system L451-8850S
FDA UDI
Class IIActive
Peridot-PT Intervertebral body fusion system L551-B846S
FDA UDI
Class IIActive
The JASPER Spinal Fixation System L117-0595
FDA UDI
Class IIActive
Peridot Intervertebral body fusion system L363-F90G
FDA UDI
Class IIActive
Peridot Intervertebral body fusion system L362-E0CC
FDA UDI
Class IIActive
Peridot Intervertebral body fusion system L362-60C6
FDA UDI
Class IIActive
Peridot Intervertebral body fusion system L362-D255
FDA UDI
Class IIActive
Peridot Intervertebral body fusion system L361-D2B6
FDA UDI
Class IIActive
Peridot Intervertebral body fusion system L361-C4A1
FDA UDI
Class IIActive
The JASPER Spinal Fixation System60 L261-60460
FDA UDI
Class IIActive
Peridot Intervertebral body fusion system L323-000B
FDA UDI
Class IIActive
The JASPER Spinal Fixation System60 L252-6065
FDA UDI
Class IIActive
The JASPER Spinal Fixation System L24B-0030
FDA UDI
Class IIActive
The JASPER Spinal Fixation System L242-8065
FDA UDI
Class IIActive
The JASPER Spinal Fixation System L230-0555
FDA UDI
Class IIActive
The JASPER Spinal Fixation System L236-6560
FDA UDI
Class IIActive
The JASPER Spinal Fixation System L22K-95105
FDA UDI
Class IIActive
The JASPER Spinal Fixation System L22K-7540
FDA UDI
Class IIActive
The JASPER Spinal Fixation System L22J-7575
FDA UDI
Class IIActive
The JASPER Spinal Fixation System L222-7065
FDA UDI
Class IIActive
PRASE-C Anterior Cervical Plate System C126-3712
FDA UDI
Class IIActive
Peridot Anterior Cervical Intervertebral Body Fusion System C22F-1715
FDA UDI
Class IIActive
The JASPER Spinal Fixation System L11G-0590
FDA UDI
Class IIActive
The JASPER Spinal Fixation System L113-9085
FDA UDI
Class IIActive
Peridot-PT Intervertebral body fusion system L541-8906S
FDA UDI
Class IIActive
Peridot-TD Anterior Cervical Intervertebral body fusion system C317-2015
FDA UDI
Class IIActive
The JASPER Spinal Fixation System L23C-9595
FDA UDI
Class IIActive
Peridot Intervertebral body fusion system L351-C2C9
FDA UDI
Class IIActive
The JASPER Spinal Fixation System L226-9035
FDA UDI
Class IIActive
The JASPER Spinal Fixation System L11B-8040
FDA UDI
Class IIActive
The JASPER Spinal Fixation System L187-5125
FDA UDI
Class IIActive
The JASPER Spinal Fixation System L158-6375
FDA UDI
Class IIActive

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