Hoya Photonics, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Hoya Photonics, Inc. - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
Denied
Hoya Photonics, Inc. has 5 FDA 510(k) cleared medical devices. Based in Fremont, US.
Historical record: 5 cleared submissions from 2004 to 2010. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Hoya Photonics, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Hoya Photonics, Inc.
5 devices
Cleared
Nov 19, 2010
REVLITE Q-SWITCHED ND: YAG LASER SYSTEM WITH NADPIECE ADAPTOR
General & Plastic Surgery
29d
Cleared
Jun 17, 2005
MEDLITE C1 Q-SWITCHED ND:YAG LASER
General & Plastic Surgery
91d
Cleared
Apr 29, 2005
DIODENT II DENTAL LASER SYSTEM
General & Plastic Surgery
81d
Cleared
Aug 05, 2004
LVI AESTHETIC LASER
General & Plastic Surgery
42d
Cleared
Apr 05, 2004
DELIGHT DENTAL ER: YAG LASER SYSTEM
General & Plastic Surgery
210d