Apex Medical Technologies, Inc.
United StatesFDA applicant, unverified FDA FEI 2025773
- Devices
- 11
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
Catalogue
Search and filter all 11 devicesCompany details
- FDA FEI number
- 2025773
- DUNS number
- 154115885
- Address
- 10064 Mesa Ridge Ct Ste 202, SAN DIEGO, CA, 92121
- [email protected]
- Phone
- 858-535-0012
Frequently asked questions
How many devices does APEX MEDICAL TECHNOLOGIES, INC. have in the registry?
The registry currently lists 11 devices for APEX MEDICAL TECHNOLOGIES, INC.. Devices recorded under merged duplicate company entries are counted once.
Which registries list APEX MEDICAL TECHNOLOGIES, INC.'s devices?
Among its 11 most recently registered devices, APEX MEDICAL TECHNOLOGIES, INC. has devices listed in FDA 510(k) (8 devices) and FDA GUDID (3 devices). A device can be listed in more than one registry, so these counts overlap.
What risk classes do APEX MEDICAL TECHNOLOGIES, INC.'s devices fall under?
Among its 11 most recently registered devices, the classes recorded for APEX MEDICAL TECHNOLOGIES, INC.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from APEX MEDICAL TECHNOLOGIES, INC. in the registry?
The most recently registered devices listed for APEX MEDICAL TECHNOLOGIES, INC. include EndosacTM ES-1, Male-FactorPakTM MFP-130, Hy-GeneTM Seminal Fluid Collection Kit ACK-121 and HI-TOUCH (TM) BRAND SURGICAL GLOVES.