# K062130: Meisinger Benex, Model BE001

- Pathway: 510(k) (Traditional)
- Applicant: Hager& Meisinger GmbH
- Decided: Apr 16, 2007 after 264 days
- Product code: EMG (Forceps, Tooth Extractor, Surgical)
- Device class: 1
- Regulation: 21 CFR 872.4565
- Recalls of this device: none
- 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.

## Indications for use
The Meisinger Benex Tooth Extraction device is to be used to extract teeth and tooth roots when traditional forceps extraction is not possible or when tooth luxation trauma to the alveolar bone is to be kept to a minimum.

Source page: https://510kreport.com/device/K062130
Methodology: https://510kreport.com/methodology