Integrated Orbital Implants, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Integrated Orbital Implants, Inc. - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
Denied
Integrated Orbital Implants, Inc. has 5 FDA 510(k) cleared medical devices. Based in La Jolla, US.
Historical record: 5 cleared submissions from 1989 to 2001. Primary specialty: Ophthalmic.
Browse the FDA 510(k) cleared devices submitted by Integrated Orbital Implants, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Integrated Orbital Implants, Inc.
5 devices
Cleared
Feb 07, 2001
BIO-EYE II ORBITAL IMPLANT
Ophthalmic
105d
Cleared
Apr 10, 2000
PERRY-KOLBERG (PK) HA-COATED TITANIUM SLEEVE
Ophthalmic
82d
Cleared
Dec 28, 1998
BIO-EYE HYDROXYAPATITE OCULAR IMPLAND AND CONFORMER
Ophthalmic
158d
Cleared
Feb 04, 1998
PERRY-KOLBERG (PK) TITANIUM MOTILITY/SUPPORT SYSTEM
Ophthalmic
86d
Cleared
Aug 24, 1989
MOTILITY ORBITAL IMPLANT
Ophthalmic
174d