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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 19 of 500

Device	Model / Reference	Registries	Class	Status
The JASPER Spinal Fixation System	L116-75115	FDA UDI	Class II	Active
The JASPER Spinal Fixation System	L112-7580	FDA UDI	Class II	Active
The JASPER Spinal Fixation System	L118-6035	FDA UDI	Class II	Active
The JASPER Spinal Fixation System	L112-6030	FDA UDI	Class II	Active
Peridot Intervertebral body fusion system	L351-4245	FDA UDI	Class II	Active
The JASPER Spinal Fixation System	L247-0065	FDA UDI	Class II	Active
The JASPER Spinal Fixation System	L23G-90115	FDA UDI	Class II	Active
The JASPER Spinal Fixation System	L23G-7050	FDA UDI	Class II	Active
The JASPER Spinal Fixation System	L21F-05120	FDA UDI	Class II	Active
The JASPER Spinal Fixation System	L210-0075	FDA UDI	Class II	Active
The JASPER Spinal Fixation System	L210-75105	FDA UDI	Class II	Active
The JASPER Spinal Fixation System	L24J-0095	FDA UDI	Class II	Active
The JASPER Spinal Fixation System	L236-0550	FDA UDI	Class II	Active
The JASPER Spinal Fixation System	L183-6110	FDA UDI	Class II	Active
Peridot Intervertebral body fusion system	L364-057H	FDA UDI	Class II	Active
The JASPER Spinal Fixation System60	L261-63490	FDA UDI	Class II	Active
The JASPER Spinal Fixation System	L236-8570	FDA UDI	Class II	Active
The JASPER Spinal Fixation System	L24K-8080	FDA UDI	Class II	Active
Peridot-PT Intervertebral body fusion system	L656-B2B2S	FDA UDI	Class II	Active
The JASPER Spinal Fixation System	L11F-0560	FDA UDI	Class II	Active
The JASPER Spinal Fixation System	L235-9580	FDA UDI	Class II	Active
The JASPER Spinal Fixation System	L228-5530	FDA UDI	Class II	Active
The JASPER Spinal Fixation System	L182-5155	FDA UDI	Class II	Active
The JASPER Spinal Fixation System	L247-7090	FDA UDI	Class II	Active
Peridot-TD Intervertebral body fusion system	L431-0034S	FDA UDI	Class II	Active
Peridot-PT Intervertebral body fusion system	L636-00A4S	FDA UDI	Class II	Active
The JASPER Spinal Fixation System	L21F-70115	FDA UDI	Class II	Active
The JASPER Spinal Fixation System	L11G-70135	FDA UDI	Class II	Active
The JASPER Spinal Fixation System	L23A-90110	FDA UDI	Class II	Active
The JASPER Spinal Fixation System	L113-5545	FDA UDI	Class II	Active
The JASPER Spinal Fixation System	L116-90100	FDA UDI	Class II	Active
The JASPER Spinal Fixation System	L11A-4545	FDA UDI	Class II	Active
Prase-C Anterior Cervical Plate System	C115-17110	FDA UDI	Class II	Active
The JASPER Spinal Fixation System	L174-3656	FDA UDI	Class II	Active
The JASPER Spinal Fixation System	L154-55130	FDA UDI	Class II	Active
The JASPER Spinal Fixation System	L171-98SS	FDA UDI	Class II	Active
The JASPER Spinal Fixation System	L117-05100	FDA UDI	Class II	Active
The JASPER Spinal Fixation System	L11C-5055	FDA UDI	Class II	Active
The JASPER Spinal Fixation System	L143-55200	FDA UDI	Class II	Active
Peridot Intervertebral body fusion system	L364-8905	FDA UDI	Class II	Active
Peridot Intervertebral body fusion system	L364-D82D	FDA UDI	Class II	Active
Peridot Intervertebral body fusion system	L322-006A	FDA UDI	Class II	Active
The JASPER Spinal Fixation System	L235-9070	FDA UDI	Class II	Active
Peridot-TD Intervertebral body fusion system	L432-00C4S	FDA UDI	Class II	Active
Peridot-TD Intervertebral body fusion system	L451-02C8S	FDA UDI	Class II	Active
Peridot-TD Intervertebral body fusion system	L451-08A0	FDA UDI	Class II	Active
Peridot-TD Intervertebral body fusion system	L441-8246	FDA UDI	Class II	Active
The JASPER Spinal Fixation System	L11H-5540	FDA UDI	Class II	Active
The JASPER Spinal Fixation System	L114-5530	FDA UDI	Class II	Active
Peridot Intervertebral body fusion system	L362-E2B5	FDA UDI	Class II	Active

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