# International Medical Devices, Inc.

- Location (FDA's records): Beverly Hills, CA
- FDA decisions: 4 (2017–2023): 4 510(k) clearances
- Product codes: MIB (4)
- Predicates its devices cite: 10 (5 its own); citations of its devices by later devices: 6 (5 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- National Medical Devices, Inc.: 2 (https://510kreport.com/company/national-medical-devices)
- Aesthetic and Reconstructive Technologies, Inc.: 2 (https://510kreport.com/company/aesthetic-and-reconstructive-technologies)
- Medisil Corporation: 1 (https://510kreport.com/company/medisil)

## Firms that cite its devices most
- Augmenta, LLC: 1 (https://510kreport.com/company/augmenta)

## Its most-cited devices
- K181387: Pre-Formed Penile Silicone Block (2019), cited by 3
- K162624: Pre-Formed Penile Silicone Block (2017), cited by 2
- K220760: Pre-Formed Penile Silicone Block (2022), cited by 1

## Recent decisions
- K223051: Pre-Formed Silicone Block (Feb 3, 2023)
- K220760: Pre-Formed Penile Silicone Block (May 13, 2022)
- K181387: Pre-Formed Penile Silicone Block (Jan 23, 2019)
- K162624: Pre-Formed Penile Silicone Block (Feb 1, 2017)

Source page: https://510kreport.com/company/international-medical-devices