Gbf Medical Group
Country not established
- Devices
- 1
What Gbf Medical Group makes
Gbf Medical Group manufactures drug insurance verification tools, urinalysis test kits, and blood/urine test kits designed for point-of-care diagnostics. These products support clinical decision-making by enabling rapid testing for substances such as drugs, hormones, or infections in urine or blood samples. The test kits are intended for use in medical offices, urgent care settings, and other healthcare environments requiring quick diagnostic results.
The company’s portfolio is classified under FDA’s Class I medical devices, which generally pose minimal risk and require compliance with 510(k) premarket notification procedures. These devices are listed in the FDA’s 510(k) database, reflecting their regulatory clearance pathway. The manufacturer operates from the United States.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Gbf Medical Group have in the registry?
The registry currently lists 1 device for Gbf Medical Group. Devices recorded under merged duplicate company entries are counted once.
Which registries list Gbf Medical Group's devices?
Among its 1 most recently registered device, Gbf Medical Group has devices listed in FDA 510(k) (1 device).
What risk classes do Gbf Medical Group's devices fall under?
Among its 1 most recently registered device, the classes recorded for Gbf Medical Group's devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Gbf Medical Group in the registry?
The most recently registered devices listed for Gbf Medical Group include DRUG, INSURANCE, URINALYSIS, BLOOD/URINE TEST KITS.