Conception Technology, Inc.
United StatesFDA applicant, unverified
- Devices
- 5
What Conception Technology, Inc. makes
Conception Technology, Inc. manufactures fertility and reproductive health devices including the ENHANCE-S PLUS, ENHANCE-S PLUS H, MICROTOOLS, ENHANCE SPERM FREEZE, and OVULON MONITOR.
The company's devices are regulated as Class I and Class II medical devices and are listed in the FDA 510(k) registry. Conception Technology, Inc. is based in the US.
Catalogue
Enhance-S Plus Ref K991322
Regimes: 510(k) Registry: 510(k)Enhance-S Plus H Ref K030116
Regimes: 510(k) Registry: 510(k)Microtools Ref K991104
Regimes: 510(k) Registry: 510(k)Enhance Sperm Freeze Ref K030117
Regimes: 510(k) Registry: 510(k)Ovulon Monitor Ref K973860
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Conception Technology, Inc. have in the registry?
The registry currently lists 5 devices for Conception Technology, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Conception Technology, Inc.'s devices?
Among its 5 most recently registered devices, Conception Technology, Inc. has devices listed in FDA 510(k) (5 devices).
What risk classes do Conception Technology, Inc.'s devices fall under?
Among its 5 most recently registered devices, the classes recorded for Conception Technology, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Conception Technology, Inc. in the registry?
The most recently registered devices listed for Conception Technology, Inc. include ENHANCE-S PLUS, ENHANCE-S PLUS H, MICROTOOLS and ENHANCE SPERM FREEZE.