Molekule, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Molekule, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Molekule Air Pro, Molekule Air Mini, Molekule Air Mini +, Molekule Air Pro RX
3
Total
3
Cleared
0
Denied
Molekule, Inc. has 3 FDA 510(k) cleared medical devices. Based in San Francisco, US.
Last cleared in 2021. Active since 2020. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Molekule, Inc. Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by Hyman, Phelps & McNamara, P.C. and Hymann, Phelps, & Mcnamara P.C..
FDA 510(k) Regulatory Record - Molekule, Inc.
3 devices