Medical Device Recalls
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1 to 8 of 8 Results
510(K) Number: K221306 |
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Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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Soltive Premium SuperPulsed Laser - Intended for incision, excision, resection, ablation, coagulatio... | 2 | 10/18/2024 | Olympus Corporation of the Americas |
Soltive Pro SuperPulsed Laser Systems-Intended for incision, excision, resection, ablation, coagulat... | 2 | 10/18/2024 | Olympus Corporation of the Americas |
Soltive Premium SuperPulsed Laser System, Model TFL-PLS | 2 | 08/05/2024 | Olympus Corporation of the Americas |
Soltive SuperPulsed Laser System Wireless Footswitch, Model TFL-AFSWL | 2 | 08/05/2024 | Olympus Corporation of the Americas |
Soltive Pro SuperPulsed Laser System, Model TFL-SLS | 2 | 08/05/2024 | Olympus Corporation of the Americas |
SOLTIVE Pro SuperPulsed Laser (TFL-SLS ) | 2 | 03/27/2024 | Olympus Corporation of the Americas |
SOLTIVE Premium SuperPulsed Laser (TFL-PLS ) | 2 | 03/27/2024 | Olympus Corporation of the Americas |
SOLTIVE SuperPulsed Laser Fibers, Model No. TFL-FBX200BS | 2 | 01/12/2024 | Olympus Corporation of the Americas |
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