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

Catalogue (50209)

Page 26 of 500

Device	Model / Reference	Registries	Class	Status
The JASPER Spinal Fixation System	L23C-6550	FDA UDI	Class II	Active
The JASPER Spinal Fixation System	L23D-8580	FDA UDI	Class II	Active
The JASPER Spinal Fixation System	L22B-6535	FDA UDI	Class II	Active
The JASPER Spinal Fixation System	L11B-70140	FDA UDI	Class II	Active
The JASPER Spinal Fixation System	L225-0560	FDA UDI	Class II	Active
The JASPER Spinal Fixation System	L185-5210	FDA UDI	Class II	Active
The JASPER Spinal Fixation System	L114-8060	FDA UDI	Class II	Active
The JASPER Spinal Fixation System	L152-63150	FDA UDI	Class II	Active
The JASPER Spinal Fixation System	L143-55200	FDA UDI	Class II	Active
Peridot Intervertebral body fusion system	L363-D242	FDA UDI	Class II	Active
The JASPER Spinal Fixation System	L185-6160	FDA UDI	Class II	Active
The JASPER Spinal Fixation System	L24K-7560	FDA UDI	Class II	Active
Peridot Intervertebral body fusion system	L351-E851	FDA UDI	Class II	Active
The JASPER Spinal Fixation System	L11A-0020	FDA UDI	Class II	Active
The JASPER Spinal Fixation System	L21M-9550	FDA UDI	Class II	Active
Peridot Intervertebral body fusion system	L323-01B6	FDA UDI	Class II	Active
Peridot-PT Intervertebral body fusion system	L531-8030S	FDA UDI	Class II	Active
Peridot-PT Intervertebral body fusion system	L523-00B9	FDA UDI	Class II	Active
The JASPER Spinal Fixation System	L185-5115	FDA UDI	Class II	Active
The JASPER Spinal Fixation System	L117-0550	FDA UDI	Class II	Active
The JASPER Spinal Fixation System	L114-05100	FDA UDI	Class II	Active
The JASPER Spinal Fixation System	L111-7020	FDA UDI	Class II	Active
The JASPER Spinal Fixation System	L23F-85110	FDA UDI	Class II	Active
The JASPER Spinal Fixation System	L11A-8070	FDA UDI	Class II	Active
The JASPER Spinal Fixation System	L219-70100	FDA UDI	Class II	Active
The JASPER Spinal Fixation System	L171-26SS	FDA UDI	Class II	Active
The JASPER Spinal Fixation System	L11E-0595	FDA UDI	Class II	Active
The JASPER Spinal Fixation System	L11C-6045	FDA UDI	Class II	Active
The JASPER Spinal Fixation System	L213-8035	FDA UDI	Class II	Active
The JASPER Spinal Fixation System	L147-63115	FDA UDI	Class II	Active
Peridot Intervertebral body fusion system	L351-40A0	FDA UDI	Class II	Active
Peridot Intervertebral body fusion system	L362-A2A4	FDA UDI	Class II	Active
The JASPER Spinal Fixation System	L11A-6055	FDA UDI	Class II	Active
Peridot Intervertebral body fusion system	L361-8045	FDA UDI	Class II	Active
The JASPER Spinal Fixation System	L22N-8580	FDA UDI	Class II	Active
The JASPER Spinal Fixation System	L161-6028	FDA UDI	Class II	Active
The JASPER Spinal Fixation System	L11F-75100	FDA UDI	Class II	Active
The JASPER Spinal Fixation System	L11E-9565	FDA UDI	Class II	Active
Peridot-TD Intervertebral body fusion system	L451-B5A0S	FDA UDI	Class II	Active
Peridot-PT Intervertebral body fusion system	L636-80C3	FDA UDI	Class II	Active
The JASPER Spinal Fixation System	L11B-95140	FDA UDI	Class II	Active
Peridot-TD Intervertebral body fusion system	L451-05B4	FDA UDI	Class II	Active
The JASPER Spinal Fixation System	L234-7075	FDA UDI	Class II	Active
The JASPER Spinal Fixation System	L22H-8055	FDA UDI	Class II	Active
The JASPER Spinal Fixation System	L24C-0545	FDA UDI	Class II	Active
The JASPER Spinal Fixation System60	L131-0001	FDA UDI	Class II	Active
The JASPER Spinal Fixation System	L23J-7085	FDA UDI	Class II	Active
The JASPER Spinal Fixation System	L222-8590	FDA UDI	Class II	Active
The JASPER Spinal Fixation System	L227-9570	FDA UDI	Class II	Active
The JASPER Spinal Fixation System	L222-6060	FDA UDI	Class II	Active

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