
Belport Company, Inc., Gingi-Pak
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Gingi-Aid Gel is an FDA 510(k)-cleared medical device (K211419) manufactured by Belport Company, Inc., Gingi-Pak. This device is classified under the Unknown specialty. FDA Device Class U. FDA clearance granted on January 9, 2022.

Ansell
SKU MSC846624

Princeton BioMeditech Corp.
SKU K014192

McKesson
SKU VM-1270030

Hollister
SKU VM-1270031