# K940261: Lynx Low-Speed Handpiece

- Pathway: 510(k) (Traditional)
- Applicant: Mti Precision Products
- Decided: Dec 29, 1994 after 342 days
- Product code: EFB (Handpiece, Air-Powered, Dental)
- Device class: 1
- Regulation: 21 CFR 872.4200
- Recalls of this device: 1 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
1 later device descends from it; 1 cites it directly.
0 of 2 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA lists a 510(k) statement for it but has not posted the file, so its predicates are not known.

## Most influential descendants
- K070001: Master Classic 5K Low Speed Handpiece, 20K Low Speed Handpiece, TM5 Low Speed Handpiece and TM20 Low Speed Handpiece (2007), 0 descendants of its own

## Recalls of this device
- May 7, 2012 · Class II · Z-2044-2014: Sharp edge on the body/housing of the Lynx TM20 TorqueMaster Low Speed Handpiece.

Source page: https://510kreport.com/device/K940261
Methodology: https://510kreport.com/methodology