Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under 2 spellings of its name, each linked to the record.
As of Nov 14, 2026, FDA's public records list MTI Precision Products with 5 510(k) clearances and 1 device recall. The most recent is a device recall dated May 7, 2012: Lynx TM20 Torquemaster Low Speed Handpiece MTI Dental Products.
| May 7, 2012 | Lynx TM20 Torquemaster Low Speed Handpiece MTI Dental ProductsClass II · Sharp edge on the body/housing of the Lynx TM20 TorqueMaster Low Speed Handpiece. | Device recalls |
| Feb 2, 2007 | MASTER CLASSIC 5K LOW SPEED HANDPIECE, 20K LOW SPEED HANDPIECE, TM5 LOW SPEED HANDPIECE AND TM20 LOW SPEED HANDPIECEK070001 · EFB | 510(k) clearances |
| Mar 28, 1996 | LYNX DPA DISPOSABLE PROPHY ANGLEK960541 · EFB | 510(k) clearances |
| Dec 29, 1994 | LYNX LOW-SPEED HANDPIECEK940261 · EFB | 510(k) clearances |
| May 15, 1990 | LYNX-SM, SCLAER DENTAL HANDPIECEK901488 · ELC | 510(k) clearances |
| Dec 18, 1989 | LYNX-HIGH SPEED HANDPIECEK895736 · EFB | 510(k) clearances |
Spellings are joined only when they reduce to the same name, or a reviewed source names the same company. Sharing an FDA establishment number (FEI) is not enough: contract sites make products for many firms. Facts marked AI were labelled by a language model from the firm's FDA names; everything else comes from FDA or Wikidata. How this page is built
