Intl., Inc.
United StatesFDA 510(k) applicant, unverified
- Devices
- 32
What Intl., Inc. makes
Genx Intl., Inc. manufactures single-lumen sideport and embryo transfer needles, embryo transfer catheters, blastocyst media and vitrification kits, sperm preparation media, buffered washing solutions for herpes treatment, human tubal fluid (HTF) supplements with and without non-essential amino acids, and microtools for reproductive procedures. The company also produces air purification systems for embryo handling and warming kits for vitrified blastocysts.
These devices are classified as Class II under FDA regulations and are supported by 510(k) clearance records. The manufacturer is based in the United States.
Catalogue
Search and filter all 32 devicesFrequently asked questions
How many devices does <Genx> Intl., Inc. have in the registry?
The registry currently lists 32 devices for <Genx> Intl., Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list <Genx> Intl., Inc.'s devices?
Among its 32 most recently registered devices, <Genx> Intl., Inc. has devices listed in FDA 510(k) (32 devices).
What risk classes do <Genx> Intl., Inc.'s devices fall under?
Among its 32 most recently registered devices, the classes recorded for <Genx> Intl., Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from <Genx> Intl., Inc. in the registry?
The most recently registered devices listed for <Genx> Intl., Inc. include <GENX> SINGLE LUMEN SIDEPORT NEEDLE, GENXCATHETER, GLOBAL BY <GENX> BLASTOCYST MEDIA and ALLGRAD WASH (HERPES BUFFERED WASHING MEDIUM).