Medical Device Manufacturer · PL , Ozorkow

Htl-Strefa S.A - FDA 510(k) Cleared Devices

7 submissions · 7 cleared · Since 2015

Total

Cleared

Denied

Htl-Strefa S.A has 7 FDA 510(k) cleared medical devices. Based in Ozorkow, PL.

Latest FDA clearance: Jul 2025. Active since 2015. Primary specialty: General Hospital.

Browse the FDA 510(k) cleared devices submitted by Htl-Strefa S.A Filter by specialty or product code using the sidebar.

Htl-Strefa S.A is one of 10 FDA 510(k) medical device manufacturers from Poland in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Htl-Strefa S.A

7 devices

1-7 of 7