Trokamed GmbH
Trokamed GmbH holds FDA 510(k) medical device clearances, first cleared 2006, most recent 2021, with 4 FDA device recalls on record.
Top product codes for Trokamed GmbH
FDA recalls by Trokamed GmbH
- Z-0715-2025 — Sheath, 18 Fr., 130 mm (REF: WA2PS18S), gastroenterology-urology endoscopic access overtube.
- Z-0713-2025 — Sheath, 20 Fr., 130 mm (REF: WA2PS20S), gastroenterology-urology endoscopic access overtube.
- Z-0716-2025 — Sheath, 18 Fr., 160 mm (REF: WA2PS18L), gastroenterology-urology endoscopic access overtube.
- Z-0714-2025 — Sheath, 20 Fr., 160 mm (REF: WA2PS20L), gastroenterology-urology endoscopic access overtube.
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 Trokamed GmbH
Data sourced from openFDA. This site is unofficial and independent of the FDA.