Copan Italia Spa is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Copan Italia Spa - FDA 510(k) Cleared Devices
Recent clearances: UriSponge™, Copan Universal Transport Medium (UTM-RT) System, Copan FecalSwab Collection, Transport and Preservation System
8
Total
8
Cleared
0
Denied
Copan Italia Spa has 8 FDA 510(k) cleared medical devices. Based in Marlborough, US.
Latest FDA clearance: Oct 2024. Active since 1997. Primary specialty: Microbiology.
Browse the FDA 510(k) cleared devices submitted by Copan Italia Spa Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Melissa M. Traylor as regulatory consultant.
FDA 510(k) Regulatory Record - Copan Italia Spa
8 devices
Cleared
Oct 11, 2024
UriSponge™
Microbiology
414d
Cleared
Apr 25, 2024
Copan Universal Transport Medium (UTM-RT) System
Microbiology
262d
Cleared
Dec 16, 2022
Copan FecalSwab Collection, Transport and Preservation System
Microbiology
344d
Cleared
Sep 17, 2020
eNAT molecular collection and preservation medium
Microbiology
73d
Cleared
Mar 23, 2018
UriSwab-Urine Collection, Transport and Preservation System
Microbiology
74d
Cleared
Apr 10, 2015
COPAN FECALSWAB COLLECTION, TRANSPORT AND PRESERVATION SYSTEM
Microbiology
252d
Cleared
Aug 20, 1997
COPAN VENTURI TRANSYSTEM AMIES MEDIUM WITHOUT CHARCOAL
Microbiology
51d
Cleared
Aug 20, 1997
COPAN VENTURI TRANSYSTEM AMIES MEDIUM WITH CHARCOAL
Microbiology
51d