# Intermed Group, Inc.

- Location (FDA's records): Lake Worth, FL
- FDA decisions: 1 (2003–2003): 1 510(k) clearance
- Product codes: HEX (1)
- Predicates its devices cite: 3 (0 its own); citations of its devices by later devices: 2 (0 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
- Vineland Medical Products, Inc.: 1 (https://510kreport.com/company/vineland-medical-products)
- Wallach Surgical Devices, Inc.: 1 (https://510kreport.com/company/wallach-surgical-devices)
- Leisegang Medical, Inc.: 1 (https://510kreport.com/company/leisegang-medical)

## Firms that cite its devices most
- United Products & Instruments, Inc.: 1 (https://510kreport.com/company/united-products-instruments)
- Gynius AB: 1 (https://510kreport.com/company/gynius)

## Its most-cited devices
- K031639: Intermed Zoom Colposcope (2003), cited by 2

## Recent decisions
- K031639: Intermed Zoom Colposcope (Aug 22, 2003)

Source page: https://510kreport.com/company/intermed-group