K. W. Griffen Co.
Country not established FDA FEI 1211177
- Devices
- 4
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
Catalogue
Fluff Gauze Bandage, Sterile & Non-Sterile Ref K953810
510(k) 510(k)Bio-Dressing, Sterile Island Dressing Ref K961098
510(k) 510(k)Bioscrub Surgical Scrub Brush Ref K870258
510(k) 510(k)Modified Use Of Triangle Bandage Sterile Ref K874161
510(k) 510(k)
Company details
- FDA FEI number
- 1211177
- Address
- 100 PEARL ST., NORWALK, CT, 06850
Frequently asked questions
How many devices does K. W. Griffen Co. have in the registry?
The registry currently lists 4 devices for K. W. Griffen Co.. Devices recorded under merged duplicate company entries are counted once.
Which registries list K. W. Griffen Co.'s devices?
Among its 4 most recently registered devices, K. W. Griffen Co. has devices listed in FDA 510(k) (4 devices).
What risk classes do K. W. Griffen Co.'s devices fall under?
Among its 4 most recently registered devices, the classes recorded for K. W. Griffen Co.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from K. W. Griffen Co. in the registry?
The most recently registered devices listed for K. W. Griffen Co. include FLUFF GAUZE BANDAGE, STERILE & NON-STERILE, BIO-DRESSING, STERILE ISLAND DRESSING, BIOSCRUB SURGICAL SCRUB BRUSH and MODIFIED USE OF TRIANGLE BANDAGE STERILE.