# K991283: Dyna Torq Torque Wrench, Torque Wrench

- Pathway: 510(k) (Traditional)
- Applicant: Micro Motors, Inc.
- Decided: Aug 18, 1999 after 125 days
- Product code: DZE (Implant, Endosseous, Root-Form)
- Device class: 2
- Regulation: 21 CFR 872.3640
- 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.
No later device cites it as a predicate yet.
0 of 1 device in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA’s file for it is a 510(k) statement, which names no predicate.

## Recalls of this device
- Jan 19, 2009 · Not classified · Z-1212-2010: Pro-Dex has initiated a recall on their Dental Torque Wrench. The recall was initiated due to an inaccurate laser etch identification of the torque value.

## Indications for use
The Dyna Torq Torque Wrench is intended for use in fastening dental implant abutments during the placement of dental implants.

Source page: https://510kreport.com/device/K991283
Methodology: https://510kreport.com/methodology