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

Catalogue (50209)

Page 23 of 500

Device	Model / Reference	Registries	Class	Status
The JASPER Spinal Fixation System	L23N-80120	FDA UDI	Class II	Active
The JASPER Spinal Fixation System	L21F-8575	FDA UDI	Class II	Active
Peridot-TD Intervertebral body fusion system	L451-8844S	FDA UDI	Class II	Active
Peridot Intervertebral body fusion system	L322-01AA	FDA UDI	Class II	Active
The JASPER Spinal Fixation System	L234-6585	FDA UDI	Class II	Active
Peridot Anterior Cervical Intervertebral Body Fusion System	C24F-1108	FDA UDI	Class II	Active
Spine Instruments	LB01-0350	FDA UDI	Class I	Active
The JASPER Spinal Fixation System	L11D-4055	FDA UDI	Class II	Active
The JASPER Spinal Fixation System	L11A-0085	FDA UDI	Class II	Active
The JASPER Spinal Fixation System	L243-95105	FDA UDI	Class II	Active
The JASPER Spinal Fixation System	L23G-0585	FDA UDI	Class II	Active
The JASPER Spinal Fixation System	L142-55180	FDA UDI	Class II	Active
The JASPER Spinal Fixation System	L141-63100	FDA UDI	Class II	Active
Peridot Intervertebral body fusion system	L361-E2B9	FDA UDI	Class II	Active
The JASPER Spinal Fixation System	L152-5550	FDA UDI	Class II	Active
The JASPER Spinal Fixation System	L114-65135	FDA UDI	Class II	Active
The JASPER Spinal Fixation System	L116-6520	FDA UDI	Class II	Active
The JASPER Spinal Fixation System	L113-70105	FDA UDI	Class II	Active
Peridot Intervertebral body fusion system	L362-C4A2	FDA UDI	Class II	Active
Peridot Intervertebral body fusion system	L361-B4CC	FDA UDI	Class II	Active
The JASPER Spinal Fixation System	L24A-0590	FDA UDI	Class II	Active
The JASPER Spinal Fixation System	L23C-9570	FDA UDI	Class II	Active
The JASPER Spinal Fixation System60	L24F-95110	FDA UDI	Class II	Active
The JASPER Spinal Fixation System	L24B-8085	FDA UDI	Class II	Active
The JASPER Spinal Fixation System	L22M-00100	FDA UDI	Class II	Active
The JASPER Spinal Fixation System	L22F-85110	FDA UDI	Class II	Active
The JASPER Spinal Fixation System	L22M-8035	FDA UDI	Class II	Active
The JASPER Spinal Fixation System	L22A-9590	FDA UDI	Class II	Active
The JASPER Spinal Fixation System	L221-0095	FDA UDI	Class II	Active
The JASPER Spinal Fixation System	L11B-75150	FDA UDI	Class II	Active
Peridot Anterior Cervical Intervertebral Body Fusion System	C247-2015	FDA UDI	Class II	Active
The JASPER Spinal Fixation System	L118-9585	FDA UDI	Class II	Active
Peridot Intervertebral body fusion system	L332-80A8	FDA UDI	Class II	Active
The JASPER Spinal Fixation System	L115-8585	FDA UDI	Class II	Active
The JASPER Spinal Fixation System	L21G-7045	FDA UDI	Class II	Active
The JASPER Spinal Fixation System	L21G-90110	FDA UDI	Class II	Active
The JASPER Spinal Fixation System	L216-05100	FDA UDI	Class II	Active
The JASPER Spinal Fixation System	L216-8535	FDA UDI	Class II	Active
The JASPER Spinal Fixation System	L177-1666	FDA UDI	Class II	Active
Peridot Intervertebral body fusion system	L351-62A1	FDA UDI	Class II	Active
The JASPER Spinal Fixation System	L172-06SS	FDA UDI	Class II	Active
The JASPER Spinal Fixation System	L11A-8555	FDA UDI	Class II	Active
The JASPER Spinal Fixation System	L11D-8080	FDA UDI	Class II	Active
Peridot Intervertebral body fusion system	L362-A2B6	FDA UDI	Class II	Active
Peridot Intervertebral body fusion system	L361-E85A	FDA UDI	Class II	Active
The JASPER Spinal Fixation System	L22M-7535	FDA UDI	Class II	Active
The JASPER Spinal Fixation System	L21K-9085	FDA UDI	Class II	Active
Peridot Intervertebral body fusion system	L351-04BC	FDA UDI	Class II	Active
The JASPER Spinal Fixation System	L23E-9555	FDA UDI	Class II	Active
The JASPER Spinal Fixation System	L21G-8080	FDA UDI	Class II	Active

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