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Medical Device

Diowave Laser System, REF: Diowave 250W

Recall date: 2026-05-20 · Source: FDA_DEVICE
Brand / Firm
Technological Medical Advancements LLC
Product
Diowave Laser System, REF: Diowave 250W
Reason for recall
Software update is needed for laser systems, for topical infrared heating to provide temporary relief of minor muscle and joint pain, spasms, stiffness associated with minor arthritis, and to temporarily increase local blood circulation, operating at a maximum average power output of 70W, which is beyond the FDA cleared 60W.
Units affected
16
Description
Diowave Laser System, REF: Diowave 250W
View official recall notice →