Scion Medical Technologies, LLC

Scion Medical Technologies, LLC holds 6 FDA 510(k) medical device clearances, first cleared 2013, most recent 2017.

Top product codes for Scion Medical Technologies, LLC

NEU — General, Plastic Surgery4 devices
KNW — Gastroenterology, Urology2 devices

Recent clearances by Scion Medical Technologies, LLC

K170905 — Star Tissue MarkerCode NEU·2017-04-27
K161234 — CASSI II Rotational Core Biopsy SystemCode KNW·2016-08-03
K153189 — Beacon Tissue Marker (SE)Code NEU·2015-12-17
K140835 — GENERAL AND PLASTIC SURGERYCode NEU·2014-05-20
K130763 — BEACON TISSUE MARKERCode NEU·2013-05-08
K123606 — CASSI II ROTATIONAL CORE BIOPSY SYSTEM; CASSI QUADPOINT DISPOSABLECode KNW·2013-03-01

Data sourced from openFDA. This site is unofficial and independent of the FDA.