# Mego Afek

- Location (FDA's records): Kfar Saba, IL
- FDA decisions: 6 (1981–2026): 6 510(k) clearances
- Names in FDA's records: Mego Afek (5); Mego Afek , Ltd. (1)
- Product codes: JOW (5), IRP (1)
- Predicates its devices cite: 5 (2 its own); citations of its devices by later devices: 11 (2 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
- Hne Healthcare, Inc.: 1 (https://510kreport.com/company/hne-healthcare)
- Huntleigh Healthcare, Inc.: 1 (https://510kreport.com/company/huntleigh-healthcare)
- Jobst Institute, Inc.: 1 (https://510kreport.com/company/jobst-institute)

## Firms that cite its devices most
- Mego Afek AC, Ltd.: 3 (https://510kreport.com/company/mego-afek-ac)
- Daesung Maref Co., Ltd.: 2 (https://510kreport.com/company/daesung-maref)
- Normatec, Inc.: 1 (https://510kreport.com/company/normatec)
- Huntleigh Healthcare, Inc.: 1 (https://510kreport.com/company/huntleigh-healthcare)
- Thermotek, Inc.: 1 (https://510kreport.com/company/thermotek)
- C-Boot, Ltd.: 1 (https://510kreport.com/company/c-boot)

## Its most-cited devices
- K013331: Lympha Press Plus Device (2001), cited by 6
- K810338: Lympha Press (1981), cited by 3
- K060220: PBS Model 701A Compression Therapy Device (2006), cited by 2

## Recent decisions
- K254267: NanoPress 760A-BT (760A-BT) (Feb 24, 2026)
- K230385: Ballancer Platinum (1222) (Apr 4, 2023)
- K072372: Phlebopress Model 601A Compression Therapy Device (Nov 21, 2007)
- K060220: PBS Model 701A Compression Therapy Device (Feb 9, 2006)
- K013331: Lympha Press Plus Device (Nov 30, 2001)
- K810338: Lympha Press (Oct 20, 1981)

Source page: https://510kreport.com/company/mego-afek