
Indiba USA, Inc.
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Indiba Diathermia Radiofrequency Device - Activ; Indiba Diathermia Radiofrequency Device - Deep Care is an FDA 510(k)-cleared medical device (K161458) manufactured by Indiba USA, Inc.. This device is classified under the General, Plastic Surgery specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on October 2, 2016. Regulation: 8.