Boyd Industries, Inc.
United Statesfrom the FDA registration address FDA establishment FEI 3001239142
- Devices
- 3
- Registrations
- FDA
- FDA recalls
- 0
What Boyd Industries, Inc. makes
Boyd Industries, Inc. manufactures the AQUA SPRAY, a device designed for water-based cleaning or cooling applications, and the BOYD DELIVERY UNIT, a system for dispensing liquids or gases in controlled environments.
These products are classified as Class I medical devices under FDA regulations and are supported by 510(k) clearance records in the U.S. registry. The company is based in the United States.
Catalogue
- Registry: GUDID
Aqua Spray Ref K971941
Regimes: 510(k) Registry: 510(k)Boyd Delivery Unit Ref K020833
Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 3001239142
- Address
- 12900 44TH ST. NORTH, CLEARWATER, FL, 33762
Frequently asked questions
How many devices does BOYD INDUSTRIES, INC. have in the registry?
The registry currently lists 3 devices for BOYD INDUSTRIES, INC.. Devices recorded under merged duplicate company entries are counted once.
Which registries list BOYD INDUSTRIES, INC.'s devices?
Among its 3 most recently registered devices, BOYD INDUSTRIES, INC. has devices listed in FDA 510(k) (2 devices) and FDA GUDID (1 device). A device can be listed in more than one registry, so these counts overlap.
What risk classes do BOYD INDUSTRIES, INC.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for BOYD INDUSTRIES, INC.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from BOYD INDUSTRIES, INC. in the registry?
The most recently registered devices listed for BOYD INDUSTRIES, INC. include Maxi S4000 Exam Chair, Power Base/Recline, Arms, Art HR, White 100-4000, AQUA SPRAY and BOYD DELIVERY UNIT.