Somatex Medical Technologies GmbH
Somatex Medical Technologies GmbH holds FDA 510(k) medical device clearances, first cleared 2008, most recent 2021, with 2 FDA device recalls on record.
Top product codes for Somatex Medical Technologies GmbH
FDA recalls by Somatex Medical Technologies GmbH
- Z-1200-2021 — Thread-like wire marker
- Z-0410-2018 — TUMARK Q, Length 12 cm, Diameter 18G, GTIN 04250195603081, REF 271500, STERILE
Recalls are matched by FDA's recalling-firm name — openFDA's enforcement dataset doesn't reference 510(k) numbers, so a recall here may cover devices beyond this company's 510(k) clearances.
Recent clearances by Somatex Medical Technologies GmbH
- K201863 — Tumark Vision, Tumark Professional, Tumark Q, Tumark Professional Q-Shape
- K182082 — Tumark for Eviva, Tumark for Brevera
- K180443 — Tumark Vision
- K111692 — TUMARK FLEX FOR MAMMOTOME,TUMARK FLEX FOR ATEC
- K102771 — BIOPSY HANDY, MRI BIOPSY HANDY
- K093064 — TUMARK PROFESSIONAL, MODEL 271560, MR-TUMARK PROFESSIONAL, MODEL 601560
- K073095 — TUMARK PROFESSIONAL, MODEL 271560; MR- TUMARK PROFESSIONAL, MODEL 601560
Data sourced from openFDA. This site is unofficial and independent of the FDA.