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GBS Commonwealth Co., Ltd.

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: —
Website: —
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PRRC Contact: —
EUDAMED SRN: —
FDA FEI Number: —
DUNS Number: 694609156

Catalogue (50209)

Page 7 of 500

Device	Model / Reference	Registries	Class	Status
Peridot-TD Intervertebral body fusion system	L451-0254	FDA UDI	Class II	Active
Peridot-PT Intervertebral body fusion system	L656-8250S	FDA UDI	Class II	Active
Peridot-PT Intervertebral body fusion system	L656-05C8	FDA UDI	Class II	Active
Peridot-TD Intervertebral body fusion system	L422-00B9S	FDA UDI	Class II	Active
The JASPER Spinal Fixation System	L142-63260	FDA UDI	Class II	Active
The JASPER Spinal Fixation System	L141-60510	FDA UDI	Class II	Active
The JASPER Spinal Fixation System	L11H-7570	FDA UDI	Class II	Active
The JASPER Spinal Fixation System	L11A-9575	FDA UDI	Class II	Active
The JASPER Spinal Fixation System	L116-85120	FDA UDI	Class II	Active
The JASPER Spinal Fixation System	L116-0525	FDA UDI	Class II	Active
Peridot Intervertebral body fusion system	L363-B571	FDA UDI	Class II	Active
Peridot Intervertebral body fusion system	L362-D2A2	FDA UDI	Class II	Active
The JASPER Spinal Fixation System	L24K-0075	FDA UDI	Class II	Active
The JASPER Spinal Fixation System60	L24G-80110	FDA UDI	Class II	Active
The JASPER Spinal Fixation System	L22M-9040	FDA UDI	Class II	Active
The JASPER Spinal Fixation System	L22A-0595	FDA UDI	Class II	Active
The JASPER Spinal Fixation System	L221-9035	FDA UDI	Class II	Active
Peridot-PT Intervertebral body fusion system	L541-8240S	FDA UDI	Class II	Active
Peridot-PT Anterior Cervical Intervertebral body fusion system	C410-2009S	FDA UDI	Class II	Active
The JASPER Spinal Fixation System	L173-4655	FDA UDI	Class II	Active
Peridot Intervertebral body fusion system	L331-00C7	FDA UDI	Class II	Active
The JASPER Spinal Fixation System	L236-9560	FDA UDI	Class II	Active
The JASPER Spinal Fixation System	L22K-8070	FDA UDI	Class II	Active
Peridot-PT Intervertebral body fusion system	L656-B8C6S	FDA UDI	Class II	Active
Peridot-TD Anterior Cervical Intervertebral body fusion system	C310-1407	FDA UDI	Class II	Active
The JASPER Spinal Fixation System	L145-6380	FDA UDI	Class II	Active
The JASPER Spinal Fixation System	L144-63260	FDA UDI	Class II	Active
The JASPER Spinal Fixation System	L12A-2631	FDA UDI	Class II	Active
Peridot Intervertebral body fusion system	L363-B244	FDA UDI	Class II	Active
Peridot Intervertebral body fusion system	L323-B145	FDA UDI	Class II	Active
Peridot Intervertebral body fusion system	L323-8108	FDA UDI	Class II	Active
Peridot Intervertebral body fusion system	L323-0083	FDA UDI	Class II	Active
Peridot Intervertebral body fusion system	L351-B246	FDA UDI	Class II	Active
The JASPER Spinal Fixation System	L156-6080	FDA UDI	Class II	Active
The JASPER Spinal Fixation System	L11F-9550	FDA UDI	Class II	Active
The JASPER Spinal Fixation System	L151-60100	FDA UDI	Class II	Active
The JASPER Spinal Fixation System	L161-6016	FDA UDI	Class II	Active
The JASPER Spinal Fixation System	L11G-9050	FDA UDI	Class II	Active
The JASPER Spinal Fixation System	L115-00100	FDA UDI	Class II	Active
The JASPER Spinal Fixation System	L24D-7595	FDA UDI	Class II	Active
The JASPER Spinal Fixation System	L231-8560	FDA UDI	Class II	Active
The JASPER Spinal Fixation System	L22N-7540	FDA UDI	Class II	Active
The JASPER Spinal Fixation System	L231-6030	FDA UDI	Class II	Active
The JASPER Spinal Fixation System	L222-0045	FDA UDI	Class II	Active
The JASPER Spinal Fixation System	L175-2656	FDA UDI	Class II	Active
The JASPER Spinal Fixation System	L16A-6325	FDA UDI	Class II	Active
The JASPER Spinal Fixation System	L12C-1838	FDA UDI	Class II	Active
The JASPER Spinal Fixation System	L143-60470	FDA UDI	Class II	Active
Peridot Intervertebral body fusion system	L364-D822	FDA UDI	Class II	Active
Peridot-PT Anterior Cervical Intervertebral body fusion system	C41A-2005S	FDA UDI	Class II	Active

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