Tuttnauer Usa Co. Ltd.
Country not established FDA establishment FEI 2435367
- Devices
- 9
- Registrations
- FDA
- FDA recalls
- 0
Catalogue
- 510(k) 510(k)
Pre-vacuum Tabletop Autoclave Ref K143311
510(k) 510(k)T-Top 10 & T-Top T-Top 11 Ref K232658
510(k) 510(k)- 510(k) 510(k)
Tuttnauer Prevacuum Table Autoclave Ref K962282
510(k) 510(k)Pre-Vacuum Autoclave With Steam Generator And Vertical Sliding Door, Models 4472 Ep-1V And 5596 Ep-1V Ref K032192
510(k) 510(k)Tuttnauer Table-Top Autoclave Ref K973550
510(k) 510(k)- 510(k) 510(k)
Tuttnauer Elara-11 Pre-Vacuum Tabletop Autoclave Ref K090783
510(k) 510(k)
Company details
- FDA FEI number
- 2435367
- Address
- 345 Oser Avenue, HAUPPAUGE, NY, 11788
Frequently asked questions
How many devices does TUTTNAUER USA CO. LTD. have in the registry?
The registry currently lists 9 devices for TUTTNAUER USA CO. LTD.. Devices recorded under merged duplicate company entries are counted once.
Which registries list TUTTNAUER USA CO. LTD.'s devices?
Among its 9 most recently registered devices, TUTTNAUER USA CO. LTD. has devices listed in FDA 510(k) (9 devices).
What risk classes do TUTTNAUER USA CO. LTD.'s devices fall under?
Among its 9 most recently registered devices, the classes recorded for TUTTNAUER USA CO. LTD.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from TUTTNAUER USA CO. LTD. in the registry?
The most recently registered devices listed for TUTTNAUER USA CO. LTD. include TUTTNAUER MINI CONTAINER CASSETTE, TUTTNAUER STANDARD CASE CASSETTE, Pre-vacuum Tabletop Autoclave, T-Top 10 & T-Top T-Top 11 and TUTTNAUER EHS SERIES TABLE-TOP AUTOCLAVE, MODEL 2540.