
Reprise Biomedical, Inc.
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MiroDry Wound Matrix is an FDA 510(k)-cleared medical device (K240277) manufactured by Reprise Biomedical, Inc.. This device is classified under the Unknown specialty. FDA Device Class U. FDA clearance granted on February 29, 2024.

Ansell
SKU MSC846624

Princeton BioMeditech Corp.
SKU K014192

McKesson
SKU VM-1270030

Hollister
SKU VM-1270031