Geotek Medikal Ltd Sti is one of 37 FDA 510(k) medical device manufacturers from Turkey in the dataset, ranked by real submission volume.
Geotek Medikal Ltd Sti - FDA 510(k) Cleared Devices
Recent clearances: Estacore-Pro Automatic Biopsy Needle, Geotek Semiautomatic Biopsy Needle, Maxicore-M Automatic Biopsy Gun Needle, Maxicore-M Automatic Biopsy Needle and Instrument
2
Total
2
Cleared
0
Denied
Geotek Medikal Ltd Sti has 2 FDA 510(k) cleared medical devices. Based in Ankara, TR.
Last cleared in 2023. Active since 2017. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Geotek Medikal Ltd Sti Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Licensale, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Geotek Medikal Ltd Sti
2 devices