Lifetek Medical, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Lifetek Medical, Inc. makes
Lifetek Medical, Inc. manufactures medical devices for assisted reproductive procedures, including the Oocyte Retrieval Needle Set (Model 90138) for egg retrieval and the Lifetek IUI Catheter for intrauterine insemination.
These devices are classified as Class II under FDA regulations and are listed in the FDA’s 510(k) clearance registry. The company is based in the United States.
Catalogue
Oocyte Retrieval Needle Set, Model 90138 Ref K992308
Regimes: 510(k) Registry: 510(k)Lifetek Iui Catheter Ref K921518
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Lifetek Medical, Inc. have in the registry?
The registry currently lists 2 devices for Lifetek Medical, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Lifetek Medical, Inc.'s devices?
Among its 2 most recently registered devices, Lifetek Medical, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Lifetek Medical, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Lifetek Medical, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Lifetek Medical, Inc. in the registry?
The most recently registered devices listed for Lifetek Medical, Inc. include OOCYTE RETRIEVAL NEEDLE SET, MODEL 90138 and LIFETEK IUI CATHETER.