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

Catalogue (50209)

Page 16 of 500

Device	Model / Reference	Registries	Class	Status
Peridot Anterior Cervical Intervertebral Body Fusion System	C21C-1410	FDA UDI	Class II	Active
The JASPER Spinal Fixation System	L11H-8535	FDA UDI	Class II	Active
The JASPER Spinal Fixation System	L11E-9075	FDA UDI	Class II	Active
The JASPER Spinal Fixation System	L11B-8530	FDA UDI	Class II	Active
The JASPER Spinal Fixation System	L114-65120	FDA UDI	Class II	Active
The JASPER Spinal Fixation System	L11B-80120	FDA UDI	Class II	Active
The JASPER Spinal Fixation System	L117-90115	FDA UDI	Class II	Active
Peridot Intervertebral body fusion system	L362-8244	FDA UDI	Class II	Active
Peridot Intervertebral body fusion system	L362-B042	FDA UDI	Class II	Active
PRASE-C Anterior Cervical Plate System	C122-3725	FDA UDI	Class II	Active
Peridot Anterior Cervical Intervertebral Body Fusion System	C21C-2009	FDA UDI	Class II	Active
The JASPER Spinal Fixation System	L11G-65110	FDA UDI	Class II	Active
The JASPER Spinal Fixation System	L114-95125	FDA UDI	Class II	Active
The JASPER Spinal Fixation System	L113-85150	FDA UDI	Class II	Active
Peridot Intervertebral body fusion system	L361-C454	FDA UDI	Class II	Active
The JASPER Spinal Fixation System	L247-9580	FDA UDI	Class II	Active
The JASPER Spinal Fixation System	L225-9050	FDA UDI	Class II	Active
The JASPER Spinal Fixation System	L11C-65120	FDA UDI	Class II	Active
The JASPER Spinal Fixation System	L11B-6025	FDA UDI	Class II	Active
The JASPER Spinal Fixation System	L11B-8020	FDA UDI	Class II	Active
The JASPER Spinal Fixation System	L218-6580	FDA UDI	Class II	Active
The JASPER Spinal Fixation System	L185-6235	FDA UDI	Class II	Active
The JASPER Spinal Fixation System	L153-6095	FDA UDI	Class II	Active
The JASPER Spinal Fixation System	L151-55200	FDA UDI	Class II	Active
The JASPER Spinal Fixation System	L11G-05105	FDA UDI	Class II	Active
Peridot Intervertebral body fusion system	L361-E841	FDA UDI	Class II	Active
Peridot Intervertebral body fusion system	L361-A2C4	FDA UDI	Class II	Active
The JASPER Spinal Fixation System	L251-55190	FDA UDI	Class II	Active
The JASPER Spinal Fixation System	L24M-9530	FDA UDI	Class II	Active
The JASPER Spinal Fixation System0	L24F-8040	FDA UDI	Class II	Active
The JASPER Spinal Fixation System	L22F-7040	FDA UDI	Class II	Active
The JASPER Spinal Fixation System	L22A-75115	FDA UDI	Class II	Active
The JASPER Spinal Fixation System	L11B-9080	FDA UDI	Class II	Active
The JASPER Spinal Fixation System	L225-0595	FDA UDI	Class II	Active
The JASPER Spinal Fixation System	L112-8025	FDA UDI	Class II	Active
The JASPER Spinal Fixation System	L22C-8055	FDA UDI	Class II	Active
The JASPER Spinal Fixation System	L226-7545	FDA UDI	Class II	Active
Peridot Intervertebral body fusion system	L343-F57B	FDA UDI	Class II	Active
The JASPER Spinal Fixation System	L223-6035	FDA UDI	Class II	Active
The JASPER Spinal Fixation System	L184-6150	FDA UDI	Class II	Active
Peridot Anterior Cervical Intervertebral Body Fusion System	C247-1707	FDA UDI	Class II	Active
Spine Instruments	LC33-0112	FDA UDI	Class I	Active
The JASPER Spinal Fixation System	L11A-90130	FDA UDI	Class II	Active
The JASPER Spinal Fixation System	L11G-9090	FDA UDI	Class II	Active
The JASPER Spinal Fixation System	L112-0570	FDA UDI	Class II	Active
Prase-C Anterior Cervical Plate System	C121-3711	FDA UDI	Class II	Active
Prase-C Anterior Cervical Plate System	C126-3719	FDA UDI	Class II	Active
Peridot Intervertebral body fusion system	L362-A8C3	FDA UDI	Class II	Active
Peridot Intervertebral body fusion system	L362-60C5	FDA UDI	Class II	Active
Peridot Intervertebral body fusion system	L362-A45B	FDA UDI	Class II	Active

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