Dlp, Inc.
United StatesFDA 510(k) applicant, unverified
- Devices
- 56
What Dlp, Inc. makes
Dlp, Inc. manufactures a range of medical devices for cardiovascular and respiratory support, including cannulas for coronary and aortic procedures, suction tubes, aspirating needles, and perfusion systems. Their portfolio also covers ventilatory accessories like infant vent catheters, blower/mister units, and venous return cannulas with integrated cuffs. Additional offerings include coronary sinus perfusion cannulas, biopsy kits, and syringes designed for guidewire placement.
The company’s devices are classified under FDA regulations as Class I and Class II, with many authorised through the 510(k) pathway. These products are listed in the FDA’s 510(k) registry, reflecting compliance with U.S. medical device regulations. The manufacturer operates from the United States.
Catalogue
Search and filter all 56 devicesShowing 1-50 of 56
Frequently asked questions
How many devices does Dlp, Inc. have in the registry?
The registry currently lists 56 devices for Dlp, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Dlp, Inc.'s devices?
Among its 50 most recently registered devices, Dlp, Inc. has devices listed in FDA 510(k) (50 devices).
What risk classes do Dlp, Inc.'s devices fall under?
Among its 50 most recently registered devices, the classes recorded for Dlp, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Dlp, Inc. in the registry?
The most recently registered devices listed for Dlp, Inc. include INFANT VENT CATHETER 12001 W/SIDE VENT, SUBMISSION CORONARY CANNULA, PERCUTANEOUS GUIDEWIRE PLACEMENT SYRINGE 50505 and CLEARVIEW BLOWER/MISTER.