Paradigm Medical Industries, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Paradigm Medical Industries, Inc. - FDA 510(k) Cleared Devices
10
Total
10
Cleared
0
Denied
Paradigm Medical Industries, Inc. has 10 FDA 510(k) cleared medical devices. Based in Salt Lake City, US.
Historical record: 10 cleared submissions from 1995 to 2005. Primary specialty: Ophthalmic.
Browse the FDA 510(k) cleared devices submitted by Paradigm Medical Industries, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Paradigm Medical Industries, Inc.
10 devices
Cleared
May 26, 2005
ULTRASONIC BIO-MICROSCOPE, MODEL P60
Radiology
37d
Cleared
Oct 21, 2002
BLOOD FLOW ANALYZER (BFA), MODEL 408-100-01
Ophthalmic
21d
Cleared
May 22, 2001
PHOTON MULTI-PLATFORM SYSTEM, MODEL Z-12834-X & Z-13175-X
General & Plastic Surgery
210d
Cleared
Dec 05, 2000
UBM PLUS, MODEL P45
Radiology
56d
Cleared
Oct 06, 2000
PHOTON MODULAR WORKSTATION SYSTEM, MODELS Z-12834-X & Z-13175-X
General & Plastic Surgery
74d
Cleared
Jun 09, 1998
QUITETIP
Ophthalmic
74d
Cleared
Jan 20, 1998
PHACOPAK
Ophthalmic
33d
Cleared
Jul 14, 1997
AUTOMATED CHAMBER MAINTENANCE MODULE
Ophthalmic
60d
Cleared
Jun 17, 1997
BLOOD FLOW ANALYZER
Ophthalmic
98d
Cleared
Oct 13, 1995
PRECISIONIST THIRTY THOUSAND
Ophthalmic
88d