Medical Device Manufacturer · US , Beverly Hills , CA

International Medical Devices, Inc. - FDA 510(k) Cleared Devices

4 submissions · 4 cleared · Since 2017

Recent clearances: Pre-Formed Silicone Block, Pre-Formed Penile Silicone Block, Pre-Formed Penile Silicone Block

Total

Cleared

Denied

International Medical Devices, Inc. has 4 FDA 510(k) cleared medical devices. Based in Beverly Hills, US.

Last cleared in 2023. Active since 2017. Primary specialty: General & Plastic Surgery.

Browse the FDA 510(k) cleared devices submitted by International Medical Devices, Inc. Filter by specialty or product code using the sidebar.

Regulatory submissions have been managed by RQM+ and Acknowledge Regulatory Strategies, LLC. 1 device has linked clinical trial registered on ClinicalTrials.gov.

International Medical Devices, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.