Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in United KingdomLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under 2 spellings of its name, each linked to the record.
As of Nov 14, 2026, FDA's public records list Endomagnetics Ltd. with 5 510(k) clearances and 2 device recalls. The most recent is a device recall dated Oct 1, 2025: Magseed Pro 12 cm soft tissue marker. Model Number: MS2-17-1-12. Product Description:….
Drug approvals, 510(k) clearances, recalls and letters, 2017 to 2026 to date
A hatched bar is a year that is not over, so its count covers only part of the year.
| Oct 1, 2025 | Magseed Pro 12 cm soft tissue marker. Model Number: MS2-17-1-12. Product Description: The Endomag Magseed Pro Magnetic Marker System is aClass II · Potential for contamination with cotton fibers. | Device recalls |
| Oct 1, 2025 | Magseed Pro 7 cm soft tissue marker. Model Number: MS2-17-1-07. Product Description: The Endomag Magseed Pro Magnetic Marker System is a Class II · Potential for contamination with cotton fibers. | Device recalls |
| Jun 28, 2024 | Magseed Pro Magnetic Marker SystemK232865 · NEU | 510(k) clearances |
| Jan 21, 2023 | Sentimag SystemK222832 · NEU | 510(k) clearances |
| Feb 16, 2018 | Magseed Magnetic Marker SysttemK173587 · NEU | 510(k) clearances |
| Jan 13, 2017 | Magseed Magnetic Marker SystemK163541 · PBY | 510(k) clearances |
| Mar 2, 2016 | Sentimag System, Sentimark Magnetic Marker SystermK153044 · PBY | 510(k) clearances |
Spellings are joined only when they reduce to the same name, or a reviewed source names the same company. Sharing an FDA establishment number (FEI) is not enough: contract sites make products for many firms. Facts marked AI were labelled by a language model from the firm's FDA names; everything else comes from FDA or Wikidata. How this page is built
