Endomagnetics Ltd.,
Endomagnetics Ltd., holds FDA 510(k) medical device clearances, first cleared 2016, most recent 2024, with 2 FDA device recalls on record.
Top product codes for Endomagnetics Ltd.,
FDA recalls by Endomagnetics Ltd.,
- Z-0317-2026 — Magseed Pro 12 cm soft tissue marker. Model Number: MS2-17-1-12. Product Description: The Endomag Magseed Pro Magnetic Marker System is a sterile, single use device composed of a marker preloaded in a 17ga Needle Delivery System. The Endomag Magseed Pro Marker is indicated for use to radiographically mark soft tissue during a surgical procedure or for future surgical procedures.
- Z-0316-2026 — Magseed Pro 7 cm soft tissue marker. Model Number: MS2-17-1-07. Product Description: The Endomag Magseed Pro Magnetic Marker System is a sterile, single use device composed of a marker preloaded in a 17ga Needle Delivery System. The Endomag Magseed Pro Marker is indicated for use to radiographically mark soft tissue during a surgical procedure or for future surgical procedures.
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 Endomagnetics Ltd.,
Data sourced from openFDA. This site is unofficial and independent of the FDA.