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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 21 of 500

Device	Model / Reference	Registries	Class	Status
The JASPER Spinal Fixation System	L241-7550	FDA UDI	Class II	Active
The JASPER Spinal Fixation System	L245-6035	FDA UDI	Class II	Active
The JASPER Spinal Fixation System	L244-85100	FDA UDI	Class II	Active
The JASPER Spinal Fixation System	L23J-9545	FDA UDI	Class II	Active
The JASPER Spinal Fixation System	L233-7530	FDA UDI	Class II	Active
The JASPER Spinal Fixation System	L221-85115	FDA UDI	Class II	Active
The JASPER Spinal Fixation System	L21K-80105	FDA UDI	Class II	Active
The JASPER Spinal Fixation System	L24B-80115	FDA UDI	Class II	Active
The JASPER Spinal Fixation System	L23C-95100	FDA UDI	Class II	Active
The JASPER Spinal Fixation System	L22F-7585	FDA UDI	Class II	Active
The JASPER Spinal Fixation System	L21M-70110	FDA UDI	Class II	Active
The JASPER Spinal Fixation System	L11C-5035	FDA UDI	Class II	Active
The JASPER Spinal Fixation System	L218-75115	FDA UDI	Class II	Active
PRASE-C Anterior Cervical Plate System	C125-4217	FDA UDI	Class II	Active
Peridot Anterior Cervical Intervertebral Body Fusion System	C220-1412	FDA UDI	Class II	Active
The JASPER Spinal Fixation System	L11C-95135	FDA UDI	Class II	Active
The JASPER Spinal Fixation System	L23M-8060	FDA UDI	Class II	Active
The JASPER Spinal Fixation System	L118-90135	FDA UDI	Class II	Active
The JASPER Spinal Fixation System	L116-9050	FDA UDI	Class II	Active
The JASPER Spinal Fixation System	L115-80135	FDA UDI	Class II	Active
The JASPER Spinal Fixation System	L113-95135	FDA UDI	Class II	Active
The JASPER Spinal Fixation System	L153-63195	FDA UDI	Class II	Active
The JASPER Spinal Fixation System	L174-066S	FDA UDI	Class II	Active
The JASPER Spinal Fixation System	L232-9080	FDA UDI	Class II	Active
Peridot-TD Anterior Cervical Intervertebral body fusion system	C310-1713	FDA UDI	Class II	Active
Peridot-TD Intervertebral body fusion system	L451-B2A4S	FDA UDI	Class II	Active
Prase-C Anterior Cervical Plate System	C116-1725	FDA UDI	Class II	Active
The JASPER Spinal Fixation System	L11E-5040	FDA UDI	Class II	Active
The JASPER Spinal Fixation System	L116-6550	FDA UDI	Class II	Active
The JASPER Spinal Fixation System	L11A-9045	FDA UDI	Class II	Active
Peridot-PT Intervertebral body fusion system	L656-85B2S	FDA UDI	Class II	Active
The JASPER Spinal Fixation System	L151-5540	FDA UDI	Class II	Active
The JASPER Spinal Fixation System	L11B-05125	FDA UDI	Class II	Active
The JASPER Spinal Fixation System	L114-4545	FDA UDI	Class II	Active
Peridot Intervertebral body fusion system	L362-045C	FDA UDI	Class II	Active
Peridot Intervertebral body fusion system	L361-A2A9	FDA UDI	Class II	Active
The JASPER Spinal Fixation System	L239-7565	FDA UDI	Class II	Active
The JASPER Spinal Fixation System	L22J-65115	FDA UDI	Class II	Active
The JASPER Spinal Fixation System	L22C-8035	FDA UDI	Class II	Active
The JASPER Spinal Fixation System	L220-6580	FDA UDI	Class II	Active
Peridot-PT Intervertebral body fusion system	L656-08B2	FDA UDI	Class II	Active
Peridot Intervertebral body fusion system	L351-8040	FDA UDI	Class II	Active
Peridot Intervertebral body fusion system	L364-D242	FDA UDI	Class II	Active
Peridot Intervertebral body fusion system	L364-0246	FDA UDI	Class II	Active
Peridot Intervertebral body fusion system	L362-E442	FDA UDI	Class II	Active
Peridot Intervertebral body fusion system	L361-D8A5	FDA UDI	Class II	Active
The JASPER Spinal Fixation System	L113-8030	FDA UDI	Class II	Active
Peridot-TD Anterior Cervical Intervertebral body fusion system	C31C-1709S	FDA UDI	Class II	Active
Spine Instruments	LA15-0109	FDA UDI	Class I	Active
The JASPER Spinal Fixation System	L183-5230	FDA UDI	Class II	Active

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