Protectaide, Inc.
United StatesFDA applicant, unverified
- Devices
- 11
What Protectaide, Inc. makes
The company manufactures single-use personal protection packs and biohazard cleanup kits designed for medical and emergency response use. These include standard personal protection packs, CPR-specific protection packs for healthcare providers, and biohazard cleanup kits for decontamination of bloodborne pathogens. The products are intended for use in clinical settings, first aid, and emergency scenarios to reduce exposure risk.
All listed devices fall under Class II regulatory classification in the US and are recorded in the FDA’s 510(k) clearance registry. The company is based in the United States, and its products are authorised under the FDA’s medical device regulations.
Catalogue
Search and filter all 11 devicesFrequently asked questions
How many devices does Protectaide, Inc. have in the registry?
The registry currently lists 11 devices for Protectaide, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Protectaide, Inc.'s devices?
Among its 11 most recently registered devices, Protectaide, Inc. has devices listed in FDA 510(k) (11 devices).
What risk classes do Protectaide, Inc.'s devices fall under?
Among its 11 most recently registered devices, the classes recorded for Protectaide, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Protectaide, Inc. in the registry?
The most recently registered devices listed for Protectaide, Inc. include PROTECTAIDE PERSONAL PROTECTION PACK NO. 12351, PROTECTAIDE PERSONAL PROTECTION PACK NO. 24592, PROTECTAIDE PERSONAL PROTECTION PACK NO. 08315 and PROTECTAIDE BIOHAZARD CLEAN-UP KIT NO. 29777.