Company ยท US
Mti Precision Products
FDA 510(k) clearances and medical device recalls filed under this name, 1989 to 2007. Name variants (Inc, Corp, punctuation) are merged.
5510(k) clearances (0 in 12 months)
1recalls (0 in 12 months)
1recalls that name a 510(k)
Product codes
Latest 510(k) clearances
| Decided | 510(k) | Device and applicant | Code |
|---|---|---|---|
| Feb 2, 2007 | K070001 | MASTER CLASSIC 5K LOW SPEED HANDPIECE, 20K LOW SPEED HANDPIECE, TM5 LOW SPEED HANDPIECE AND TM20 LOW SPEED HANDPIECE Mti Precision Products | EFB |
| Mar 28, 1996 | K960541 | LYNX DPA DISPOSABLE PROPHY ANGLE Mti Precision Products | EFB |
| Dec 29, 1994 | K940261 | LYNX LOW-SPEED HANDPIECE Mti Precision Products | EFB |
| May 15, 1990 | K901488 | LYNX-SM, SCLAER DENTAL HANDPIECE Mti Precision Products | ELC |
| Dec 18, 1989 | K895736 | LYNX-HIGH SPEED HANDPIECE Mti Precision Products | EFB |
Latest recalls
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Jul 12, 2014 | MTI Precision Products LLC. Lynx TM20 Torquemaster Low Speed Handpiece MTI Dental Products Terminated |
EFB | K940261 |