
By:
Sr. Marketing Manager, Midmark Dental
Steam sterilization is one of the most widely used methods for instrument processing in dentistry, using saturated steam under pressure to kill microorganisms, including spores. For sterilization to be effective and compliant, the full cycle must complete—including the final drying phase.
Some dental team members may not realize that drying is a required part of the sterilization process. It’s not optional. When instrument packs come out of the sterilizer damp or wet, it’s not just an inconvenience, it compromises sterility. Moisture allows microorganisms to travel from the outside of the packaging to the instruments inside, breaching the sterile barrier (Purdue CRCST).
That’s why, according to ANSI/AAMI ST79 guidance (as summarized in sterile processing education materials), any pack that is wet or damp after sterilization should be considered contaminated.
Every wet pack in your sterilizer load triggers additional steps. Since “[w]et packages are not considered sterile,” they must be “identified, repackaged, and re-sterilized” (totalmedicalcompliance.com).
If wet packs aren’t caught immediately, contaminated instruments may end up in clinical use, putting patients at risk. If they are caught, teams can still lose time reprocessing instruments, waiting for instruments to become available and adjusting patient schedules.
Pack dryness is essential for safety, yet many dental teammates are not aware of its importance or that it’s absolutely required.
Wet packs can result from several factors:
Avoiding these issues means following validated instructions for use (IFU), loading trays properly (paper side down, no layering, using a pouch rack when possible) and choosing sterilizers with optimized airflow and real-time cycle guidance.

Next-generation Midmark M9® and M11® Steam Sterilizers are purpose-built to minimize drying issues and prevent workflow disruptions. Features support drying consistency, user accountability and adherence to best practices.
Key features include:
Independent evaluations also highlight the importance of effective drying and accountability in the sterilization process. In a Dental Advisor evaluation, drying performance and user tracking were specifically called out as Midmark sterilizer strengths. One clinician noted:
“Dries instruments completely and records all cycle information, while also tracking which user has removed instruments from the sterilizer.”
Features like these do more than check regulatory boxes—they help teams monitor usage, ensure cycle completion and prevent missteps in shared sterilization environments.
Dry packs do more than check a box—they help preserve the chain of sterility from autoclave to patient. Sterile-processing training guidance identifies removal of wet packs from the sterilizer as a common mistake that can lead to patient safety issues, additional workload and audit flags.
On the other hand, practices that consistently achieve dry packs can:
Midmark sterilizers are designed to help simplify the sterilization process—from loading to final drying—and help your team work smarter, not harder.
Contact us to explore how Midmark sterilizers can help you reduce sterilization issues and support best-in-class clinical workflows.