# E & M Engineering, Inc.

- Location (FDA's records): Richmond, VA
- FDA decisions: 6 (1993–1999): 6 510(k) clearances
- Product codes: GEI (5), HGI (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 5 (0 its own)
- Recalls linked to its devices: 3 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms that cite its devices most
- Medtek Devices, Inc.: 1 (https://510kreport.com/company/medtek-devices)
- Wallach Surgical Devices, Inc.: 1 (https://510kreport.com/company/wallach-surgical-devices)
- Erbe USA, Inc.: 1 (https://510kreport.com/company/erbe-usa)
- Conmed Corporation: 1 (https://510kreport.com/company/conmed)
- Geiger Medical Technologies, Inc.: 1 (https://510kreport.com/company/geiger-medical-technologies)

## Its most-cited devices
- K936304: Electrosurgical Pencil (1994), cited by 3
- K936075: Reusable, Hand Controlled Esp (1994), cited by 1
- K945531: Blade Electrode (1995), cited by 1

## Recent decisions
- K984276: Disposable Electrosurgery Grounding Pad (Feb 10, 1999)
- K952030: Loop/Square Electrode (Jul 31, 1996)
- K945531: Blade Electrode (Feb 10, 1995)
- K936304: Electrosurgical Pencil (Jun 13, 1994)
- K936075: Reusable, Hand Controlled Esp (Jun 6, 1994)
- K921271: Electrosurgical Unit (Jul 2, 1993)

Source page: https://510kreport.com/company/e-m-engineering