Solos Ophthalmology is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Solos Ophthalmology - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
Denied
Solos Ophthalmology has 5 FDA 510(k) cleared medical devices. Based in Norcross, US.
Historical record: 5 cleared submissions from 1987 to 1988. Primary specialty: Ophthalmic.
Browse the FDA 510(k) cleared devices submitted by Solos Ophthalmology Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Solos Ophthalmology
5 devices
Cleared
Jan 11, 1988
SOLOS SINGLE USE TITANIUM TIP
Ophthalmic
81d
Cleared
Aug 10, 1987
SOLOS EYESITE CAP SLEEVE
Ophthalmic
35d
Cleared
Jul 31, 1987
SOLOS EYESITE CANNULAS
Ophthalmic
25d
Cleared
Jul 31, 1987
SOLOS EYESITE SPONGES
Ophthalmic
25d
Cleared
Jul 31, 1987
SOLOS EYESITE DRAPES
General Hospital
25d