Dryden Corp.
United StatesFDA 510(k) applicant, unverified
- Devices
- 21
What Dryden Corp. makes
Dryden Corp. manufactures medical devices for respiratory and anesthesia systems, including disposable and reusable components like breathing circuits, bacterial filters, and airway management tools. Their product line covers valve systems such as the Bag-Tail Bleed Valve and Universal Tourniquet, as well as specialized interfaces like the Scratch & Sniff for anesthesia administration. Fixed connectors, inflatable masks, and reusable non-conductive Y-adapters are also part of their offerings.
The company’s devices are classified under FDA’s Class I and Class II categories, with regulatory clearance via the 510(k) pathway. Products are listed in the FDA’s 510(k) database, and the manufacturer operates from the United States.
Catalogue
Search and filter all 21 devicesFrequently asked questions
How many devices does Dryden Corp. have in the registry?
The registry currently lists 21 devices for Dryden Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Dryden Corp.'s devices?
Among its 21 most recently registered devices, Dryden Corp. has devices listed in FDA 510(k) (21 devices).
What risk classes do Dryden Corp.'s devices fall under?
Among its 21 most recently registered devices, the classes recorded for Dryden Corp.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Dryden Corp. in the registry?
The most recently registered devices listed for Dryden Corp. include BAG-TAIL BLEED VALVE, UNIVERSAL TOURNIQUET, DRYDEN SCAVENGER INTERFACE SYSTEM and BREATHING CIRCUIT W/HEATED WIRE.