Cpac, Inc.
United StatesFDA applicant, unverified
- Devices
- 5
What Cpac, Inc. makes
Cpac, Inc. manufactures dental and laboratory sterilization equipment, including dry heat sterilizers and power units for vacuum-assisted sterilization systems. Their portfolio also includes portable vacuum units designed for dental office use, alongside reusable dental instruments and trays processed through these systems.
The company’s products are regulated under FDA’s 510(k) clearance process, with devices classified as Class I and Class II. These sterilization systems and accessories are listed in the FDA’s 510(k) database, adhering to US medical device regulations. The manufacturer is based in the United States.
Catalogue
Steri-Dent, Steri-Sure Ref K110867
Regimes: 510(k) Registry: 510(k)Dry Heat Sterilizer Ref K771070
Regimes: 510(k) Registry: 510(k)Steri-Vac Power Units Ref K781486
Regimes: 510(k) Registry: 510(k)Steri-Dent, Steri-Sure Ref K094026
Regimes: 510(k) Registry: 510(k)Porto-Vac Ref K771071
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Cpac, Inc. have in the registry?
The registry currently lists 5 devices for Cpac, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Cpac, Inc.'s devices?
Among its 5 most recently registered devices, Cpac, Inc. has devices listed in FDA 510(k) (5 devices).
What risk classes do Cpac, Inc.'s devices fall under?
Among its 5 most recently registered devices, the classes recorded for Cpac, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Cpac, Inc. in the registry?
The most recently registered devices listed for Cpac, Inc. include STERI-DENT, STERI-SURE, DRY HEAT STERILIZER, STERI-VAC POWER UNITS and PORTO-VAC.