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

Catalogue (50209)

Page 17 of 500

Device	Model / Reference	Registries	Class	Status
Peridot Intervertebral body fusion system	L322-0064	FDA UDI	Class II	Active
The JASPER Spinal Fixation System	L24K-5540	FDA UDI	Class II	Active
The JASPER Spinal Fixation System	L24J-8570	FDA UDI	Class II	Active
The JASPER Spinal Fixation System	L236-85120	FDA UDI	Class II	Active
The JASPER Spinal Fixation System	L111-9565	FDA UDI	Class II	Active
Peridot-PT Intervertebral body fusion system	L656-02B8S	FDA UDI	Class II	Active
Peridot-TD Intervertebral body fusion system	L451-8540S	FDA UDI	Class II	Active
Peridot-PT Anterior Cervical Intervertebral body fusion system	C417-1714S	FDA UDI	Class II	Active
The JASPER Spinal Fixation System	L12D-1638	FDA UDI	Class II	Active
The JASPER Spinal Fixation System	L11H-75115	FDA UDI	Class II	Active
The JASPER Spinal Fixation System	L148-60135	FDA UDI	Class II	Active
The JASPER Spinal Fixation System	L11E-65115	FDA UDI	Class II	Active
Peridot Intervertebral body fusion system	L362-8840	FDA UDI	Class II	Active
Peridot Intervertebral body fusion system	L361-84B6	FDA UDI	Class II	Active
Peridot Intervertebral body fusion system	L361-C4C6	FDA UDI	Class II	Active
The JASPER Spinal Fixation System	L251-55480	FDA UDI	Class II	Active
The JASPER Spinal Fixation System	L24E-9035	FDA UDI	Class II	Active
The JASPER Spinal Fixation System	L24F-8595	FDA UDI	Class II	Active
The JASPER Spinal Fixation System	L249-0555	FDA UDI	Class II	Active
The JASPER Spinal Fixation System	L22G-0030	FDA UDI	Class II	Active
The JASPER Spinal Fixation System	L227-6545	FDA UDI	Class II	Active
The JASPER Spinal Fixation System	L221-8070	FDA UDI	Class II	Active
Peridot-PT Intervertebral body fusion system	L551-02A6S	FDA UDI	Class II	Active
Peridot Intervertebral body fusion system	L361-E056	FDA UDI	Class II	Active
Peridot Intervertebral body fusion system	L361-D241	FDA UDI	Class II	Active
Peridot-TD Intervertebral body fusion system	L431-00A7S	FDA UDI	Class II	Active
The JASPER Spinal Fixation System	L240-6555	FDA UDI	Class II	Active
The JASPER Spinal Fixation System	L23C-7060	FDA UDI	Class II	Active
The JASPER Spinal Fixation System	L244-0040	FDA UDI	Class II	Active
The JASPER Spinal Fixation System	L22F-6040	FDA UDI	Class II	Active
The JASPER Spinal Fixation System	L22M-7590	FDA UDI	Class II	Active
The JASPER Spinal Fixation System	L22A-7080	FDA UDI	Class II	Active
The JASPER Spinal Fixation System	L224-9040	FDA UDI	Class II	Active
The JASPER Spinal Fixation System	L142-55530	FDA UDI	Class II	Active
The JASPER Spinal Fixation System	L141-55450	FDA UDI	Class II	Active
The JASPER Spinal Fixation System	L113-9055	FDA UDI	Class II	Active
Peridot Intervertebral body fusion system	L361-C2B2	FDA UDI	Class II	Active
The JASPER Spinal Fixation System	L24E-8030	FDA UDI	Class II	Active
The JASPER Spinal Fixation System	L24B-05100	FDA UDI	Class II	Active
The JASPER Spinal Fixation System	L240-90110	FDA UDI	Class II	Active
The JASPER Spinal Fixation System	L22M-0550	FDA UDI	Class II	Active
The JASPER Spinal Fixation System	L22N-0075	FDA UDI	Class II	Active
The JASPER Spinal Fixation System	L21H-00105	FDA UDI	Class II	Active
Peridot Intervertebral body fusion system	L323-A0AB	FDA UDI	Class II	Active
The JASPER Spinal Fixation System	L11A-00150	FDA UDI	Class II	Active
The JASPER Spinal Fixation System	L116-7095	FDA UDI	Class II	Active
The JASPER Spinal Fixation System	L115-8085	FDA UDI	Class II	Active
The JASPER Spinal Fixation System	L115-6545	FDA UDI	Class II	Active
The JASPER Spinal Fixation System	L113-6050	FDA UDI	Class II	Active
Peridot Intervertebral body fusion system	L361-60C7	FDA UDI	Class II	Active

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