G Surgical LLC
US Last updated 25 Oct 2026
- Devices
- 12
- Registries
- GUDIDFDA 510(k)FDA
- FDA recalls
- 0
Catalogue
GPS Anterior Cervical Plate System CSS-04012 Ref CSS-04012
GPS Anterior Cervical Plate System CTL-41893 Ref CTL-41893
GPS Anterior Cervical Plate System CSS-01803 Ref CSS-01803
G Surgical Marksman MIS System Ref K240737
G Surgical Marksman System Ref K193219
GPS Spacers Ref K142456
G Surgical OCT Spinal System Ref K171834
G Surgical Marksman Spinal Deformity System Ref K230063
GPS Cervical Spacers Ref K210890
Gps, G Surgical Pedicle System Ref K081041
G Surgical Marksman MIS System Ref K161516
FDA establishments
- G Surgical Co., Ltd. BANGKOK Krung Thep Maha Nakhon · TH FEI 3006378738
What G Surgical LLC makes
G Surgical LLC manufactures bone-screw internal spinal fixation systems. Their product portfolio includes the GPS Anterior Cervical Plate System.
These devices are classified as Class II medical devices and are listed in the FDA UDI database. The company is based in the United States.
Frequently asked questions
What type of medical devices does G Surgical LLC manufacture?
G Surgical LLC specializes in the production of bone-screw internal spinal fixation systems. Their current product portfolio includes the GPS Anterior Cervical Plate System, which is designed for internal spinal fixation procedures.
Where is G Surgical LLC based?
G Surgical LLC is based in the United States. This location information is provided to help users identify the geographic origin of the manufacturer and their associated regulatory oversight.
How are the devices from G Surgical LLC classified?
The devices manufactured by G Surgical LLC, such as the GPS Anterior Cervical Plate System, are classified as Class II medical devices. This classification is based on the regulatory framework used to categorize the risk profile of medical equipment.
Where can I find information about the devices produced by this company?
The devices manufactured by G Surgical LLC are listed in the FDA UDI database. This registry is the official source for identifying specific medical devices and their regulatory status within the United States.
Information
- Country
- US
- Address
- 9433 Bee Cave Road, Austin, TX, 78733
- FDA FEI number
- 3009169872