Dornier Medtech America, Inc.
FDA 510(k) & PMA Approved Devices — 37 products
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Total Devices37
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K221903 | Delta III Pro | LNS | 2023-02-22 | View |
| 510(k) | K213252 | Dornier Thulio | GEX | 2022-07-27 | View |
| 510(k) | K220871 | Nautilus | JAA | 2022-04-18 | View |
| 510(k) | K210394 | Electrosurgical accessory | FAS | 2021-05-19 | View |
| 510(k) | K201815 | Dornier MAGELLAN Ureteral Access Sheath | FED | 2020-11-20 | View |
| 510(k) | K201074 | Delta III Lithotripter | LNS | 2020-09-03 | View |
| 510(k) | K190612 | EQUINOX Balloon Dilatation Catheter | EZN | 2019-12-06 | View |
| 510(k) | K190312 | Dornier Ureteral Stent | FAD | 2019-11-15 | View |
| 510(k) | K191187 | Dornier MINNOW Ureteral Catheter | EYB | 2019-09-18 | View |
| 510(k) | K172084 | Delta III Lithotripter | LNS | 2017-08-08 | View |
| 510(k) | K161771 | Medilas H Laser Fibers | GEX | 2016-07-28 | View |
| 510(k) | K130344 | DORNIER MEDILAS UROPULSE | GEX | 2013-03-21 | View |
| 510(k) | K122159 | DORNIER MEDILAS H30 SOLVO | GEX | 2013-02-01 | View |
| 510(k) | K122768 | GENESIS | JAA | 2013-01-18 | View |
| 510(k) | K123385 | MEDILAS H LASER FIBERS | GEX | 2012-12-14 | View |
| 510(k) | K121656 | GEMINI LITHOTRIPTER | LNS | 2012-09-24 | View |
| 510(k) | K121938 | MEDILAS H RFID LASER FIBER | GEX | 2012-08-01 | View |
| 510(k) | K110364 | DORNIER MEDILAS D LITEBEAM+ 1470 | GEX | 2011-12-07 | View |
| 510(k) | K083500 | MEDILAS D FAMILY LASERS, INCLUDING MEDILAS D LITEBEAM, LITEBEAM +, UROBEAM, MULTIBEAM, FLEXIPULSE AND MAGNAPULSE | GEX | 2009-02-12 | View |
| 510(k) | K083258 | MEDILAS D FAMILY LASERS, INCLUDING MEDILAS D LITEBEAM, LITEBEAM +, UROBEAM, MULTIBEAM, FLEXIPULSE AND MAGNAPULSE | GEX | 2009-01-30 | View |
No matching devices.
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