# Mk-Dent GmbH

- Location (FDA's records): Kumhausen, DE
- FDA decisions: 2 (2003–2005): 2 510(k) clearances
- Product codes: EFB (2)
- Predicates its devices cite: 5 (1 its own); citations of its devices by later devices: 2 (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
- Handpiece Unlimited: 2 (https://510kreport.com/company/handpiece-unlimited)
- A-Dec, Inc.: 1 (https://510kreport.com/company/a-dec)
- Ritter Co.: 1 (https://510kreport.com/company/ritter)

## Firms that cite its devices most
- Osseo Scientific, LLC: 1 (https://510kreport.com/company/osseo-scientific)

## Its most-cited devices
- K051872: MK-Dent Low Speed Handpieces and Accessories Including Spare Parts, Tubings, and Light Power System, Models:  LS2011 (2005), cited by 1
- K032234: MK-Dent High Speed Dental Handpiece, Models HS 4021K, 4011K, 4012K, and HS 6021K, 6011K, 6012K (2003), cited by 1

## Recent decisions
- K051872: MK-Dent Low Speed Handpieces and Accessories Including Spare Parts, Tubings, and Light Power System, Models:  LS2011 (Oct 3, 2005)
- K032234: MK-Dent High Speed Dental Handpiece, Models HS 4021K, 4011K, 4012K, and HS 6021K, 6011K, 6012K (Oct 2, 2003)

Source page: https://510kreport.com/company/mk-dent