Regulatory & Marketing Services, Inc.
United StatesFDA applicant, unverified
- Devices
- 22
What Regulatory & Marketing Services, Inc. makes
The company manufactures single-use and reusable medical devices for urinary catheterization, including urethral catheters, Foley catheterization kits, and pediatric Foley catheters, as well as silicone-coated catheters and suction catheter kits with sterile saline. It also produces orthopedic supports like dynamic elbow orthoses, tracheostomy tubes with disposable inner cannulas, and central line dressing change trays. Sharps containers, pre-filled syringes (e.g., acetic acid), and pain management devices are part of its portfolio.
The device portfolio spans FDA-regulated Class I, Class II, and Class III categories, with submissions recorded in the FDA’s 510(k) clearance registry. The company is based in the United States and adheres to U.S. medical device regulations.
Catalogue
Search and filter all 22 devicesFrequently asked questions
How many devices does Regulatory & Marketing Services, Inc. have in the registry?
The registry currently lists 22 devices for Regulatory & Marketing Services, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Regulatory & Marketing Services, Inc.'s devices?
Among its 22 most recently registered devices, Regulatory & Marketing Services, Inc. has devices listed in FDA 510(k) (22 devices).
What risk classes do Regulatory & Marketing Services, Inc.'s devices fall under?
Among its 22 most recently registered devices, the classes recorded for Regulatory & Marketing Services, Inc.'s devices are Class I, Class II and Class III. Each device page shows its own class and authorisation.
What are the newest devices from Regulatory & Marketing Services, Inc. in the registry?
The most recently registered devices listed for Regulatory & Marketing Services, Inc. include ORION RED URETHRAL CATHETER, PAIN DOC, DIAL MEDICAL SUPPLY SHARPS CONTAINER and ACCUFLEX DYNAMIC ELBOW ORTHOSIS.