Lerner Medical Devices, Inc. is one of 21599 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Lerner Medical Devices, Inc. - FDA 510(k) Cleared Devices
Recent clearances: LH-75 PHOTOTHERAPY SYSTEM, LH-75T PHOTOTHERAPY SYSTEM, LEVIA PHOTOTHERAPY SYSTEM
3
Total
3
Cleared
0
Denied
Lerner Medical Devices, Inc. has 3 FDA 510(k) cleared medical devices. Based in Los Angeles, US.
Historical record: 3 cleared submissions from 2004 to 2009. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Lerner Medical Devices, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Entela, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Lerner Medical Devices, Inc.
3 devices