Vapocoolshot, Inc
United StatesFDA applicant, unverified FDA FEI 3021853802
Vapocoolshot, Inc is a medical device manufacturer, with 24 devices listed in FDA GUDID and FDA 510(k) (FDA Unclassified and Class II) as of 15 Nov 2026.
- Devices
- 24
- Registrations
- FDA
- FDA recalls
- 0
Registry facts
- Registries
- FDA GUDID 21
- FDA 510(k) 3
- Device classes
- FDA Unclassified 23
- FDA Class II 1
- Identifiers
- FDA FEI 3021853802
- DUNS 032313444
At a glance
Market reach
- United States
- FDA FEI
Catalogue
Search and filter all 24 devicesCompany details
- FDA FEI number
- 3021853802
- DUNS number
- 032313444
- Address
- 950 Peninsula Corporate Circle, Boca Raton, FL, 33487
- Phone
- 1-833-266-5528
Frequently asked questions
How many devices does Vapocoolshot, Inc have in the registry?
The registry currently lists 24 devices for Vapocoolshot, Inc. Devices recorded under merged duplicate company entries are counted once.
Which registries list Vapocoolshot, Inc's devices?
Among its 24 most recently registered devices, Vapocoolshot, Inc has devices listed in FDA 510(k) (3 devices) and FDA GUDID (21 devices). A device can be listed in more than one registry, so these counts overlap.
What risk classes do Vapocoolshot, Inc's devices fall under?
Among its 24 most recently registered devices, the classes recorded for Vapocoolshot, Inc's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Vapocoolshot, Inc in the registry?
The most recently registered devices listed for Vapocoolshot, Inc include DentalJect Applicator DJ01000-00, DentalJect Syringe Connector DJ02000-00, DentalJect Starter Kit - No Syringe Connector DJ06000-00 and DentalJect Single Kit DJ01300-00.