# Medisurg, Ltd.

- Location (FDA's records): Norristown, PA
- FDA decisions: 4 (2000–2007): 4 510(k) clearances
- Product codes: NCR (3), EKZ (1)
- Predicates its devices cite: 4 (3 its own); citations of its devices by later devices: 7 (3 its own)
- Recalls linked to its devices: 1 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Wallach Surgical Devices, Inc.: 1 (https://510kreport.com/company/wallach-surgical-devices)

## Firms that cite its devices most
- Lensar, Inc.: 1 (https://510kreport.com/company/lensar)
- Mynosys Cellular Devices, Inc.: 1 (https://510kreport.com/company/mynosys-cellular-devices)
- Oertli Instrumente AG: 1 (https://510kreport.com/company/oertli-instrumente)
- Lensx Lasers, Inc.: 1 (https://510kreport.com/company/lensx-lasers)

## Its most-cited devices
- K001498: The Fugo Blade (2000), cited by 5
- K041019: The Fugo Blade for Glaucoma (2004), cited by 1
- K050933: Fugo Blade for Peripheral Iridotomy, Model M300 (2005), cited by 1

## Recent decisions
- K063468: The Fugo Blade for Dentistry (Apr 18, 2007)
- K050933: Fugo Blade for Peripheral Iridotomy, Model M300 (Dec 9, 2005)
- K041019: The Fugo Blade for Glaucoma (Oct 8, 2004)
- K001498: The Fugo Blade (Aug 10, 2000)

Source page: https://510kreport.com/company/medisurg