K W Griffen Co

FDA Filings

This page includes the latest FDA filings for K W Griffen Co. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.

FDA Registration(s)
Registration Number1211177
FEI Number1211177
NameK. W. GRIFFEN CO.
Owner & OperatorK. W. GRIFFEN CO.
Contact Address100 PEARL ST. --
Norwalk CT 06850 US
Official Correspondent
  • JAMES C BROWN
  • x-203-8461923-x
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration Address100 PEARL ST.
NORWALK, CT 06850 US
Establishment TypeManufacture Medical Device



FDA Filings

Device
Company
DeviceDate
BioMed Systems, Inc., K. W. Griffen Company, BioMed Systems
Otc Medication2021-12-23
BioMed Systems, Inc., K. W. Griffen Company, BioMed Systems
Otc Medication2019-11-12
BioMed Systems, Inc., K. W. Griffen Company, BioMed Systems
Otc Medication2012-09-06
K. W. GRIFFEN CO.
BIO-DRESSING, STERILE ISLAND DRESSING1996-05-03
K. W. GRIFFEN CO.
FLUFF GAUZE BANDAGE, STERILE & NON-STERILE1995-09-14
K. W. GRIFFEN CO.
STERILE SCRUB BRUSH1992-08-27
K. W. GRIFFEN CO.
MODIFIED USE OF TRIANGLE BANDAGE STERILE1987-12-04
K. W. GRIFFEN CO.
BIOSCRUB SURGICAL SCRUB BRUSH1987-02-24

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