Medical Device Manufacturer · IL , Efrat 90962

Terraflex - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 1994

Total

Cleared

Denied

Terraflex has 1 FDA 510(k) cleared medical devices. Based in Efrat 90962, IL.

Historical record: 1 cleared submissions from 1994 to 1994. Primary specialty: Dental.

Browse the FDA 510(k) cleared devices submitted by Terraflex Filter by specialty or product code using the sidebar.

Terraflex is one of 267 FDA 510(k) medical device manufacturers from Israel in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Terraflex

1 devices

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