Adeor Medical AG
Valley Bavaria, DE
ADEOR MEDICAL AG appears in FDA device records in Valley Bavaria, DE. FDA records list 4 510(k) clearances between and , no PMA records and one registered establishment. As of , FDA records show no recalls for this company, and at least one establishment registration is current.
FDA records held for this company
510(k) clearance history
FDA records hold 4 510(k) clearances for Adeor Medical AG between 2014 and 2026. The busiest year on record is 2014, with 1. The most recent is 2026, with 1.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 2014 | 1 |
| 2020 | 1 |
| 2021 | 1 |
| 2026 | 1 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K253772 | Velocity Alpha MR High Speed Surgical Drill System | HBB | Substantially Equivalent | |
| K191479 | Velocity Alpha Highspeed Surgical Drill System | HBE | Substantially Equivalent | |
| K191847 | Adeor Medical nxt Non-stick Bipolar Forceps, Adeor Medical nxt Single-Use Non-stick Bipolar Forceps | GEI | Substantially Equivalent | |
| K130755 | HICUT HIGHSPEED INSTRUMENT | HBE | Substantially Equivalent |
Registered establishments
| Registration | FEI | Establishment | Address | Registration expires | Product codes listed |
|---|---|---|---|---|---|
| 3007031059 | 3007031059 | ADEOR MEDICAL AG | Martinshof 5, Valley Bavaria D-83626 DE | 2026 |
Registration numbers link to the FDA registration and listing record for that establishment.
FDA product codes
Recall records
No recall records for this company in the ingested FDA data.
Verification record
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Data as of , FDA export datePage updated Source: openFDA, public domain