Cutter Laboratories, Inc.
United StatesFDA 510(k) applicant, unverified
- Devices
- 41
What Cutter Laboratories, Inc. makes
Cutter Laboratories, Inc. manufactures respiratory devices such as the EXERCISOR, as well as over-the-needle catheters for medical procedures. The company also produces surgical tools like carbide burs, acrylic trays for implant setups, and silicone impression mats for dental or medical impressions. Additional offerings include urine meters, peritoneal dialysis trays, and dosimetric release programs for administration sets, alongside medical accessories like suture guides and mini centrifuges.
The company’s products are regulated under FDA classifications, including Class I, Class II, and Class III devices, with many authorised via the 510(k) pathway. These devices are listed in the FDA’s 510(k) registry, and the manufacturer is based in the United States.
Catalogue
Search and filter all 41 devicesFrequently asked questions
How many devices does Cutter Laboratories, Inc. have in the registry?
The registry currently lists 41 devices for Cutter Laboratories, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Cutter Laboratories, Inc.'s devices?
Among its 41 most recently registered devices, Cutter Laboratories, Inc. has devices listed in FDA 510(k) (41 devices).
What risk classes do Cutter Laboratories, Inc.'s devices fall under?
Among its 41 most recently registered devices, the classes recorded for Cutter Laboratories, 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 Cutter Laboratories, Inc. in the registry?
The most recently registered devices listed for Cutter Laboratories, Inc. include EXERCISOR, RESPIRATORY, CATHETERS, OVER-THE-NEEDLE, CUTTER RESIFLEX FOLEY CATHETERS and CUTTER TRAY-ACRYLIC FOR IMP TRAYS.