Balfour, Inc.
United StatesFDA applicant, unverified
- Devices
- 3
What Balfour, Inc. makes
Balfour, Inc. manufactures antimicrobial and sterile stockinette products, including the Burlington Antimicrobial Stockinette, Burlington Sterile Antimicrobial Stock, and Burlington Stockinette.
These devices are classified as Class II medical devices and are listed in the FDA 510(k) registry; the company is based in the United States.
Catalogue
Burlington Antimicrobial Stockineette Ref K833122
Regimes: 510(k) Registry: 510(k)Burlington Sterile Antimicrobial Stock Ref K833121
Regimes: 510(k) Registry: 510(k)Burlington Stockinette Ref K822770
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Balfour, Inc. have in the registry?
The registry currently lists 3 devices for Balfour, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Balfour, Inc.'s devices?
Among its 3 most recently registered devices, Balfour, Inc. has devices listed in FDA 510(k) (3 devices).
What risk classes do Balfour, Inc.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Balfour, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Balfour, Inc. in the registry?
The most recently registered devices listed for Balfour, Inc. include BURLINGTON ANTIMICROBIAL STOCKINEETTE, BURLINGTON STERILE ANTIMICROBIAL STOCK and BURLINGTON STOCKINETTE.