Dlp, Inc.
United StatesFDA 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 devicesCuatico Myelography Needles Ref K813367
Regimes: 510(k) Registry: 510(k)Aortic Root Cannula Ref K790565
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
Cardiopulmonary Bypass Ref K810820
Regimes: 510(k) Registry: 510(k)Maxx 470 Core Biopsy Gun Ref K900082
Regimes: 510(k) Registry: 510(k)Angiography Needle W/Wo Connection Ref K840923
Regimes: 510(k) Registry: 510(k)
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