Air Techniques, Inc.
Active in EUDAMEDUnited Statesfrom SRN EUDAMED FDA SRN US-MF-000052811 FEI 2428225
Air Techniques, Inc. is a medical device manufacturer based in the United States, with 208 devices listed in FDA GUDID, FDA 510(k) and EUDAMED (FDA Class I and II; EU Class I) as of 13 Nov 2026.
- Devices
- 208
- Registrations
- EUDAMEDFDA
- FDA recalls
- 0
Registry facts
- Registries
- FDA GUDID 190
- FDA 510(k) 18
- EUDAMED 11
- Device classes
- FDA Class I 167
- FDA Class II 39
- EU Class I 1
- Top EMDN categories
- Identifiers
- EUDAMED SRN US-MF-000052811
- FDA FEI 2428225
- DUNS 043835081
At a glance
Market reach
- European Union
- EUDAMED actor
- United States
- FDA FEI
Catalogue
Search and filter all 208 devicesShowing 1-50 of 208
Company details
- EUDAMED SRN
- US-MF-000052811
- FDA FEI number
- 2428225
- DUNS number
- 043835081
- EUDAMED status
- Active
- EUDAMED registered name
- Air Techniques, Inc.
- EUDAMED abbreviated name
- ATI
- Registered address
- 1295, Walt Whitman Road, 11747, Melville, New York, United States
- Website
- www.airtechniques.com/
- facebook.com/AirTechniques
- Phone
- +1 516 2145510
- PRRC contact
- Mardonio Nicolas
From the company website
Paving the way with compelling, reliable dental products, ensuring today’s dental professionals are Equipped for Life. Air Techniques is a leading manufacturer of robust mechanical systems, intuitive digital imaging systems, and highly effective hygiene products for all application areas. Our customers include dental experts from private practices to clinics and universities at every scale. We are committed to being a dependable partner to every one of our customers, delivering the best products and solutions to meet individual needs.
Frequently asked questions
How many devices does Air Techniques, Inc. have in the registry?
The registry currently lists 208 devices for Air Techniques, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Air Techniques, Inc.'s devices?
Among its 50 most recently registered devices, Air Techniques, Inc. has devices listed in EUDAMED (5 devices) and FDA GUDID (49 devices). A device can be listed in more than one registry, so these counts overlap.
What risk classes do Air Techniques, Inc.'s devices fall under?
Among its 50 most recently registered devices, the classes recorded for Air Techniques, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Air Techniques, Inc. in the registry?
The most recently registered devices listed for Air Techniques, Inc. include VistaScan Ultra View, VistaScan Ultra View Accessory Kit 2170100601, ScanX Duo Touch J1205E and ScanX Duo Touch J1205R.