# Handpiece Unlimited

- Location (FDA's records): Luebeck, DE
- FDA decisions: 1 (2002–2002): 1 510(k) clearance
- Product codes: EBF (1)
- Predicates its devices cite: 1 (0 its own); citations of its devices by later devices: 4 (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
- Ritter Co.: 1 (https://510kreport.com/company/ritter)

## Firms that cite its devices most
- Mk-Dent GmbH: 2 (https://510kreport.com/company/mk-dent)
- Delma Medical Instrument (Guangzhou) Co., Ltd.: 1 (https://510kreport.com/company/delma-medical-instrument-guangzhou)
- Beyes Dental Canada, Inc.: 1 (https://510kreport.com/company/beyes-dental-canada)

## Its most-cited devices
- K021250: MK-Dent Push Button Highspeed Handpiece, 4 Holes, Models HS 2012 (Standard Head) & HS 2014 (Small Head) (2002), cited by 4

## Recent decisions
- K021250: MK-Dent Push Button Highspeed Handpiece, 4 Holes, Models HS 2012 (Standard Head) & HS 2014 (Small Head) (Oct 24, 2002)

Source page: https://510kreport.com/company/handpiece-unlimited