Best Labs
Country not established
- Devices
- 4
What Best Labs makes
Best Labs manufactures single-use, disposable medical devices designed for surgical and procedural applications, including the Model S (surgical instrument), Model M (minimally invasive tool), Model P (procedural accessory), and Model C (cauterization device). These products are intended for one-time use in controlled clinical settings to assist in precision tasks.
The company’s portfolio is regulated under FDA Class I devices, with each model authorised via the 510(k) clearance pathway. Devices are listed in the FDA’s 510(k) database, and the manufacturer operates from the United States.
Catalogue
Best Labs Model S Ref K903473
Regimes: 510(k) Registry: 510(k)Best Labs Model M Ref K903472
Regimes: 510(k) Registry: 510(k)Best Labs Model P Ref K903471
Regimes: 510(k) Registry: 510(k)Best Labs Model C Ref K903474
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Best Labs have in the registry?
The registry currently lists 4 devices for Best Labs. Devices recorded under merged duplicate company entries are counted once.
Which registries list Best Labs's devices?
Among its 4 most recently registered devices, Best Labs has devices listed in FDA 510(k) (4 devices).
What risk classes do Best Labs's devices fall under?
Among its 4 most recently registered devices, the classes recorded for Best Labs's devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Best Labs in the registry?
The most recently registered devices listed for Best Labs include BEST LABS MODEL S, BEST LABS MODEL M, BEST LABS MODEL P and BEST LABS MODEL C.