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LED RED Light Therapy Panel

Model RV200A · Shenzhen RedV Medical Equipment CO., LTD · DI 06977717371201

ILYLamp, Infrared, Therapeutic Heating · Class II · 21 CFR 890.5500

UDILibrary device dossier · generated 2026-09-12 · sources: FDA GUDID, openFDA (recalls, MAUDE, 510(k)/PMA), FDA Data Dashboard (inspections, compliance actions), 510(k) summary documents.

Recall history (0)

No recalls linked in the loaded window.

Adverse-event reports — MAUDE (0)

Caveat (required reading): MAUDE report counts cannot be used to compute incidence rates or compare device safety. Reporting is incomplete, duplicated, and spikes with publicity; there is no denominator of devices in use. The peer line is a reporting baseline (average device in the same product code), not a risk measure.

5914182019-03: 0 reports for this device; peer average 1.67/device2019-07: 0 reports for this device; peer average 2/device2019-10: 0 reports for this device; peer average 1/device2020-02: 0 reports for this device; peer average 2/device2020-03: 0 reports for this device; peer average 2/device2020-04: 0 reports for this device; peer average 2/device2021-07: 0 reports for this device; peer average 1/device2023-01: 0 reports for this device; peer average 1/device2023-03: 0 reports for this device; peer average 2/device2023-12: 0 reports for this device; peer average 1/device2024-03: 0 reports for this device; peer average 2/device2024-04: 0 reports for this device; peer average 4/device2024-05: 0 reports for this device; peer average 2/device2024-06: 0 reports for this device; peer average 2/device2024-11: 0 reports for this device; peer average 1/device2024-12: 0 reports for this device; peer average 1/device2025-02: 0 reports for this device; peer average 4/device2025-03: 0 reports for this device; peer average 2/device2025-04: 0 reports for this device; peer average 1.5/device2025-05: 0 reports for this device; peer average 2/device2025-06: 0 reports for this device; peer average 2/device2025-07: 0 reports for this device; peer average 1.5/device2025-09: 0 reports for this device; peer average 1.5/device2025-10: 0 reports for this device; peer average 2.5/device2025-11: 0 reports for this device; peer average 4/device2026-02: 0 reports for this device; peer average 12/device2026-03: 0 reports for this device; peer average 18/device2026-06: 0 reports for this device; peer average 6/device03071002030407010312030405061112020304050607091011020306
Monthly adverse-event reports for this device versus the product-code average.
MonthThis device (reports)Product-code average (reports per device)
2019-0301.67
2019-0702
2019-1001
2020-0202
2020-0302
2020-0402
2021-0701
2023-0101
2023-0302
2023-1201
2024-0302
2024-0404
2024-0502
2024-0602
2024-1101
2024-1201
2025-0204
2025-0302
2025-0401.5
2025-0502
2025-0602
2025-0701.5
2025-0901.5
2025-1002.5
2025-1104
2026-02012
2026-03018
2026-0606
This device (reports/month)Average device in ILY (reports/device/month)

Regulatory clearances

  • None linked in the loaded window.

Manufacturer compliance record — Shenzhen RedV Medical Equipment CO., LTD

Nothing in the loaded window.