Hermes Medical Solutions AB
Hermes Medical Solutions AB holds FDA 510(k) medical device clearances, first cleared 2012, most recent 2026, with 1 FDA device recall on record.
Top product codes for Hermes Medical Solutions AB
FDA recalls by Hermes Medical Solutions AB
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 Hermes Medical Solutions AB
- K253835 — Affinity
- K252477 — Hybrid Viewer (00859873006240)
- K243919 — Voxel Dosimetry (00859873006226)
- K241364 — Hybrid Viewer (00859873006189)
- K202882 — Affinity
- K193152 — Affinity
- K191216 — Voxel Dosimetry v1.0
- K181468 — Hybrid3D
- K171681 — Hermes Medical Imaging Suite v5.7
- K171719 — Hybrid3D
- K163687 — OLINDA EXM
- K163394 — Hybrid3D
- K153056 — Hermes Medical Imaging Suite v5.6
- K142631 — Hermes Medical Imaging Suite v5.5
- K140269 — HERMES MEDICAL IMAGING SUITE V5.4
- K131233 — HERMES MEDICAL IMAGING SUITE V5.3
- K121278 — HERMES MEDICAL IMAGING SUITE V5.2
Data sourced from openFDA. This site is unofficial and independent of the FDA.