Tri-Med Specialties, Inc.
United StatesFDA applicant, unverified
- Devices
- 14
What Tri-Med Specialties, Inc. makes
Tri-Med Specialties, Inc. manufactures medical devices for diagnostic and therapeutic procedures in gastrointestinal and esophageal care, including paracentesis trays, retrieval forceps, paracentesis needles and cannulas, esophageal dilators, gastric lavage systems, endoscopic fluid introduction catheters, rectal tubes, and suction catheters. Their products are designed for fluid management, tissue retrieval, and dilation in clinical settings.
The company’s portfolio consists of Class II devices, regulated under the FDA’s 510(k) clearance pathway. These devices are listed in the FDA’s 510(k) registry, reflecting their compliance with U.S. medical device regulations. The manufacturer is based in the United States.
Catalogue
Search and filter all 14 devicesFrequently asked questions
How many devices does Tri-Med Specialties, Inc. have in the registry?
The registry currently lists 14 devices for Tri-Med Specialties, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Tri-Med Specialties, Inc.'s devices?
Among its 14 most recently registered devices, Tri-Med Specialties, Inc. has devices listed in FDA 510(k) (14 devices).
What risk classes do Tri-Med Specialties, Inc.'s devices fall under?
Among its 14 most recently registered devices, the classes recorded for Tri-Med Specialties, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Tri-Med Specialties, Inc. in the registry?
The most recently registered devices listed for Tri-Med Specialties, Inc. include TRI-MED PARACENTESIS TRAY, T-RX RETRIEVAL FORCEPS, PARACENTESIS NEEDLES/CANNULAS and PATTISON ESOPHAGEAL DILATOR.