Infinitech, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Infinitech, Inc. - FDA 510(k) Cleared Devices
6
Total
6
Cleared
0
Denied
Infinitech, Inc. has 6 FDA 510(k) cleared medical devices. Based in Chesterfield, US.
Historical record: 6 cleared submissions from 1994 to 1997. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Infinitech, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Infinitech, Inc.
6 devices
Cleared
Oct 01, 1997
INFINITECH BULLET ENDO ILLUMINATED PICK MANIPULATOR
Ophthalmic
90d
Cleared
Aug 01, 1997
INFINITECH MULTI-SPOT SLIT LAMP LASER ADAPTER
Ophthalmic
65d
Cleared
Oct 19, 1995
INFINITECH HIGH INTENSITY XENON LIGHT SOURCE SYSTEM
Ophthalmic
195d
Cleared
Mar 01, 1994
INFINITECH OTOPROBE
General & Plastic Surgery
358d
Cleared
Feb 09, 1994
END-IRRIGATING ENDOILLUMINATOR
General & Plastic Surgery
317d
Cleared
Feb 07, 1994
INFINITECH BREATH EZ
General & Plastic Surgery
87d