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THOR Photomedicine Ltd

9 FDA 510(k) clearances · Recalling firm

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RecordFirmDate
Brand Name: THOR Product Name: NovoTHOR Model/Catalog Number: S2188 Software Version: N/A recall (Z-2416-2025)THOR Photomedicine Ltd2025-08-22
Brand Name: THOR Product Name: NovoTHOR XL Model/Catalog Number: S2190 Software Version: N recall (Z-2417-2025)THOR Photomedicine Ltd2025-08-22
Brand Name: THOR Product Name: NovoTHOR Gen 3.0 Reg PRX Model/Catalog Number: S2189 Softwa recall (Z-2418-2025)THOR Photomedicine Ltd2025-08-22
Brand Name: THOR Product Name: NovoTHOR Gen 3.0 Reg PRX Model/Catalog Number: S2186 Softwa recall (Z-2419-2025)THOR Photomedicine Ltd2025-08-22
NovoTHOR Whole Body Light Pod, Gen 3.0 (1) Product Code S2188 - Reg (2) Product Code S2189 recall (Z-0972-2024)THOR Photomedicine Ltd2024-02-01
NovoTHOR Gen 2.0 whole body red light therapy bed, model S1176 recall (Z-0453-2024)Thor Photomedicine Ltd2023-12-01
G041 POD, THOR NOVO GEN 2.0 XL whole body red light therapy bed, model S1177 recall (Z-0454-2024)Thor Photomedicine Ltd2023-12-01
NovoTHOR Gen 2.5 Regular whole body red light therapy bed, model S2183 recall (Z-0455-2024)Thor Photomedicine Ltd2023-12-01
NovoTHOR Gen 2.5 XL whole body red light therapy bed, model S2184. recall (Z-0456-2024)Thor Photomedicine Ltd2023-12-01

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Every clearance here is in the API, with alerts when new ones post.