Beacon Converters, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Beacon Converters, Inc. makes
Beacon Converters, Inc. manufactures sterilization indicators and seal protectors, including self-seal pouches designed for medical sterilization processes. These products are used to verify the integrity of sterilized packages and ensure proper sealing before use in healthcare settings.
The company’s portfolio is regulated under FDA Class II devices, with products listed via the 510(k) pathway. These devices are intended for use in the United States, where compliance with FDA requirements is mandatory.
Catalogue
Sterilization Indicator/Seal Protector Ref K811408
Regimes: 510(k) Registry: 510(k)Steriledge Self Seal Pouch Ref K810469
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Beacon Converters, Inc. have in the registry?
The registry currently lists 2 devices for Beacon Converters, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Beacon Converters, Inc.'s devices?
Among its 2 most recently registered devices, Beacon Converters, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Beacon Converters, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Beacon Converters, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Beacon Converters, Inc. in the registry?
The most recently registered devices listed for Beacon Converters, Inc. include STERILIZATION INDICATOR/SEAL PROTECTOR and STERILEDGE SELF SEAL POUCH.