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Sign in to claim this brandOlsen Medical
US
Last updated May 23, 2026
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Catalogue (1255)
Page 1 of 26| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Symmetry Olsen | 80430 | FDA UDI | Class II | Active |
| Symmetry Olsen | 20-0321R | FDA UDI | Class II | Active |
| Symmetry Olsen | 10-0481I | FDA UDI | Class II | Active |
| Symmetry Olsen | 67514 | FDA UDI | Class II | Active |
| Symmetry Olsen | 90-9502 | FDA UDI | Class II | Active |
| Symmetry Olsen | 66014 | FDA UDI | Class II | Active |
| Symmetry Olsen | 20-1440K | FDA UDI | Class II | Active |
| Symmetry Olsen | 90-9008 | FDA UDI | Class II | Active |
| Symmetry Olsen | 10-1203I | FDA UDI | Class II | Active |
| Symmetry Olsen | 20-1162I | FDA UDI | Class II | Active |
| Symmetry Olsen | 20-1384KI-28 | FDA UDI | Class II | Active |
| Symmetry Olsen | 66306 | FDA UDI | Class II | Active |
| Symmetry Olsen | 30-0012 | FDA UDI | Class II | Active |
| Symmetry Olsen | 20-1315K | FDA UDI | Class II | Active |
| Symmetry Olsen | 20-1180K | FDA UDI | Class II | Active |
| Symmetry Olsen | 97152 | FDA UDI | Class II | Active |
| Symmetry Olsen | 42203 | FDA UDI | Class II | Active |
| Symmetry Olsen | 69500 | FDA UDI | Class II | Active |
| Symmetry Olsen | 68601 | FDA UDI | Class II | Active |
| Symmetry Olsen | 20-1360 | FDA UDI | Class II | Active |
| Symmetry Olsen | 20-1563KI | FDA UDI | Class II | Active |
| Symmetry Olsen | 20-1160 | FDA UDI | Class II | Active |
| Symmetry Olsen | 90-80004 | FDA UDI | Class II | Active |
| Symmetry Olsen | 41604 | FDA UDI | Class II | Active |
| Symmetry Olsen | 20-5370K-28 | FDA UDI | Class II | Active |
| Symmetry Olsen | 87400 | FDA UDI | Class II | Active |
| Symmetry Olsen | 41300 | FDA UDI | Class II | Active |
| Symmetry Olsen | 66305 | FDA UDI | Class II | Active |
| Symmetry Olsen | 80000 | FDA UDI | Class II | Active |
| Symmetry Olsen | 12102 | FDA UDI | Class II | Active |
| Symmetry Olsen | 10-1331 | FDA UDI | Class II | Active |
| Symmetry Olsen | 80304-C | FDA UDI | Class II | Active |
| Symmetry Olsen | 80505 | FDA UDI | Class II | Active |
| Symmetry Olsen | 97136BX | FDA UDI | Class II | Active |
| Symmetry Olsen | 97154BX | FDA UDI | Class II | Active |
| Symmetry Olsen | 10-1486I | FDA UDI | Class II | Active |
| Symmetry Olsen | 20-1200K-28 | FDA UDI | Class II | Active |
| Symmetry Olsen | 10-0361I | FDA UDI | Class II | Active |
| Symmetry Olsen | 10-0331I | FDA UDI | Class II | Active |
| Symmetry Olsen | 97171 | FDA UDI | Class II | Active |
| Symmetry Olsen | 43204 | FDA UDI | Class II | Active |
| Symmetry Olsen | 42500 | FDA UDI | Class II | Active |
| Symmetry Olsen | 30-1011S | FDA UDI | Class II | Active |
| Symmetry Olsen | 40-1102 | FDA UDI | Class II | Active |
| Symmetry Olsen | 77000 | FDA UDI | Class II | Active |
| Symmetry Olsen | 20-1330KI | FDA UDI | Class II | Active |
| Symmetry Olsen | 08-0204 | FDA UDI | Class II | Active |
| Symmetry Olsen | 66201 | FDA UDI | Class II | Active |
| Symmetry Olsen | 20-0421R-39 | FDA UDI | Class II | Active |
| Symmetry Olsen | 10-1200I | FDA UDI | Class II | Active |
Related Companies
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FDA Recalls (6)
Recalls reported by this firm to the FDA. Listed at company level — FDA recall records don't identify a specific catalogue device.
| Date | Recall No. | Class | Status | Reason |
|---|---|---|---|---|
| May 11, 2018 | Z-1942-2018 | — | terminated | Products may encroach into the sterile pouch seal thereby increasing the risk of the seal being compromised. |
| May 11, 2018 | Z-1941-2018 | — | terminated | Products may encroach into the sterile pouch seal thereby increasing the risk of the seal being compromised. |
| May 11, 2018 | Z-1943-2018 | — | terminated | Products may encroach into the sterile pouch seal thereby increasing the risk of the seal being compromised. |
| May 11, 2018 | Z-1945-2018 | — | terminated | Products may encroach into the sterile pouch seal thereby increasing the risk of the seal being compromised. |
| May 11, 2018 | Z-1944-2018 | — | terminated | Products may encroach into the sterile pouch seal thereby increasing the risk of the seal being compromised. |
| Aug 29, 2006 | Z-0182-2007 | — | terminated | Testing conducted by the firm indicates that electrodes identified with certain part numbers may fall out from the electrosurgical pencil or handle presenting the potential for harm or injury to the patient and/or user. |