Inntec, Inc.
United StatesFDA applicant, unverified
- Devices
- 3
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Iui Catheter, Model 9057 Ref K052059
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Inntec, Inc. have in the registry?
The registry currently lists 3 devices for Inntec, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Inntec, Inc.'s devices?
Among its 3 most recently registered devices, Inntec, Inc. has devices listed in FDA 510(k) (3 devices).
What risk classes do Inntec, Inc.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Inntec, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Inntec, Inc. in the registry?
The most recently registered devices listed for Inntec, Inc. include IUI CATHETER, MODEL 9057, EMBRYO TRANSFER CATHETER WITH ACCESSORY STYLET, MODELS 9018, 9023, 9018-S, 9023-S and OOCYTE RETRIEVAL NEEDLE SET, MODELS 917-IH AND 917-SH.