Silent Nite Sleep Appliance recall — FDA Z-2769-2026
Due to device not having FDA Clearance
Overview of recall records associated with Prismatik Dentalcraft, Inc., including dates, categories and classifications where available.
Classification mix: Class II: 1.
Due to device not having FDA Clearance
This page summarizes recall records in which the official source identifies Prismatik Dentalcraft, Inc. as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.
Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.