<Genx> Intl., Inc.

FDA Regulatory Profile

<Genx> Intl., Inc. appears in FDA public data with 0 recalls, 24 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on May 3, 2012.

Summary

Total Recalls
0
510(k) Clearances
24
Inspections
0
Compliance Actions
0

Known Names

genx intl, <genx> intl

Recent 510(k) Clearances

K-NumberDeviceDate
K112083LIFEGLOBAL TOTAL, TOTAL FOR FERTILIZATION, TOTAL W/HEPES, HTF TOTAL, HTF TOTAL W/HEPESMay 3, 2012
K080395SUNIVF DISHESAugust 13, 2008
K053552GLOBAL FERTILIZATION, EMBRYO CULTURE AND TRANSFER MEDIAMay 19, 2006
K053551MICROMANIPULATION MEDIA SYSTEM, LG HYALURONIDASE AND LG PARAFFIN OILMay 9, 2006
K040530MEDIA CULTURE SYSTEMJune 25, 2004
K023033ALLGRAD WASH (HERPES BUFFERED WASHING MEDIUM)November 26, 2002
K022590PVP (POLYVINYLPYRROLIDONE)August 30, 2002
K022334HTF PLUS - HTF WITH NON-ESSENTIAL AMINO ACIDSAugust 28, 2002
K022547ACIDIFIED TYRODES SOLUTIONAugust 28, 2002
K022352HTF PLUS WITH HEPES (HTF WITH NON-ESSENTIAL AMINO ACIDS)August 28, 2002
K022330ALLGRAD 45 AND 90 CELL SEPARATION MEDIAAugust 26, 2002
K022332LITE MINERAL OILAugust 23, 2002
K022335ALLGRAD AND ALLGRAD100August 23, 2002
K010183GLOBAL BY <GENX> BLASTOCYST MEDIAMay 2, 2001
K001600<GENX> CODA INCUBATOR CELLMATENovember 22, 2000
K001486GENX CODA AIR PURIFICATION SYSTEMSeptember 15, 2000
K993881GENX CULTURE DISHFebruary 14, 2000
K993884GENX MICROTOOLSFebruary 14, 2000
K991266<GENX> EMBRYO TRANSFER CATHETER CC GLIDERSeptember 9, 1999
K991264<GENX> SINGLE LUMEN SIDEPORT NEEDLESeptember 9, 1999