Suretek Medical is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Suretek Medical - FDA 510(k) Cleared Devices
4
Total
4
Cleared
0
Denied
Suretek Medical has 4 FDA 510(k) cleared medical devices. Based in Greenville, US.
Historical record: 4 cleared submissions from 2006 to 2006. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Suretek Medical Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Suretek Medical
4 devices
Cleared
May 17, 2006
SURETEK MEDICAL REPROCESSED COMPRESSION SLEEVES
Cardiovascular
231d
Cleared
May 12, 2006
SURETEK REPROCESSED LAPAROSCOPIC INSTRUMENTS
General & Plastic Surgery
226d
Cleared
May 10, 2006
SURETEK MEDICAL REPROCESSED ELECTROSURGICAL ELECTRODES
General & Plastic Surgery
224d
Cleared
May 10, 2006
SURETEK MEDICAL REPROCESSED ARTHROSCOPIC BLADES AND BURS
General & Plastic Surgery
224d