# NTI-KAHLA GMBH, ROTARY DENTAL INSTRUMENTS

FEI: 3002515789
Status: Active
Establishment types: Repack or Relabel Medical Device; Manufacture Medical Device
Owner/operator: NTI-KAHLA GMBH, ROTARY DENTAL INSTRUMENTS (#9022916)

Address: IM CAMISCH 3, KAHLA Thuringia, D-07768, DE

Mandatory US Agent: Emergo Global Representation LLC

## Products

Total registered: 1
Top product codes: DZA
Regulation §: 872.4130

Proprietary names: NTI Endo Root facers, NTI T Endo Drill, NTI, NTI Gates Glidden drills, NTI Peeso reamers

## Source

- openFDA: https://api.fda.gov/device/registrationlisting.json?search=registration.fei_number:%223002515789%22
- FDA Registration Lookup: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm?lid=3002515789