Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in SwitzerlandLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field., part of Johnson & JohnsonLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under 4 spellings of its name, each linked to the record. See the Johnson & Johnson group view.
As of Nov 15, 2026, FDA's public records list Medos International Sàrl with 101 510(k) clearances and 2 device recalls. The most recent is a device recall dated Jul 23, 2026: Velys Enabling Tech Robotic-Assist Station REF: 451611001.
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.
| Jul 23, 2026 | Velys Enabling Tech Robotic-Assist Station REF: 451611001Class II · Software issue within robotic controller which may cause unintended movement of the robotic arm during bone preparation | Device recalls |
| Feb 2, 2024 | CERENOVUS CEREBASE DA Guide Sheath, Part Numbers: a) GS9080SD; b) GS9090SD; c) GS9095SD; Vascular guide-catheter, single-useClass I · Medos has received an increase in complaints for CEREBASE DA Guide Sheath with reports of fractures at the distal end, w | Device recalls |
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
