# Verimed Holdings, Inc.

- Location (FDA's records): Fort Lauderdale, FL
- FDA decisions: 12 (1983–1998): 12 510(k) clearances
- Product codes: HCC (5), HIR (3), IPF (3), KQX (1)
- Predicates its devices cite: 2 (1 its own); citations of its devices by later devices: 6 (1 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
- Perrymeter Systems: 1 (https://510kreport.com/company/perrymeter-systems)

## Firms that cite its devices most
- Empi: 2 (https://510kreport.com/company/empi)
- Chattanooga Group, Inc.: 1 (https://510kreport.com/company/chattanooga-group)
- Regulatory Strategies, Inc.: 1 (https://510kreport.com/company/regulatory-strategies)
- Mega Electronics, Ltd.: 1 (https://510kreport.com/company/mega-electronics)

## Its most-cited devices
- K832714: Verimed Myoexorciser (1983), cited by 2
- K892649: Verimed Myoexorciser Iii (Myo Iii) (1989), cited by 2
- K913912: Verimed Perineometer (1992), cited by 1
- K893220: Verimed Myoexorciser Veristim (1990), cited by 1

## Recent decisions
- K981277: Periform (Nov 20, 1998)
- K954127: Biofeedback Device (Nov 14, 1995)
- K951969: Myoexorciser II Fual (Jun 14, 1995)
- K930670: Phyaction 787 (Jul 2, 1993)
- K922550: Romas (Range of Motion Assessment System) (Dec 10, 1992)
- K913912: Verimed Perineometer (Jun 16, 1992)
- K893220: Verimed Myoexorciser Veristim (Mar 7, 1990)
- K892649: Verimed Myoexorciser Iii (Myo Iii) (Dec 13, 1989)

Source page: https://510kreport.com/company/verimed-holdings