Nitinol Medical Technologies, Inc.
United StatesFDA applicant, unverified
- Devices
- 7
What Nitinol Medical Technologies, Inc. makes
Nitinol Medical Technologies, Inc. manufactures the Simon Nitinol Filter and its associated straight line delivery systems. These devices are designed for use as vena cava filters.
The company is based in the United States, and its products are classified as Class II medical devices. These devices are listed in the FDA 510(k) regulatory registry.
Catalogue
Simon Nitinol Filter/Straight Line System Ref K963014
Regimes: 510(k) Registry: 510(k)Simon Nitinol Filter/Straight Line System Ref K970099
Regimes: 510(k) Registry: 510(k)Simon Nitinol Filter, Modification Ref K912144
Regimes: 510(k) Registry: 510(k)Simon Nitinol Filter Ref K940489
Regimes: 510(k) Registry: 510(k)Simon Nitinol Filter Ref K944353
Regimes: 510(k) Registry: 510(k)Simon Nitinol Filter System Ref K963016
Regimes: 510(k) Registry: 510(k)Simon Nitinol Filter Ref K894703
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Nitinol Medical Technologies, Inc. have in the registry?
The registry currently lists 7 devices for Nitinol Medical Technologies, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Nitinol Medical Technologies, Inc.'s devices?
Among its 7 most recently registered devices, Nitinol Medical Technologies, Inc. has devices listed in FDA 510(k) (7 devices).
What risk classes do Nitinol Medical Technologies, Inc.'s devices fall under?
Among its 7 most recently registered devices, the classes recorded for Nitinol Medical Technologies, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Nitinol Medical Technologies, Inc. in the registry?
The most recently registered devices listed for Nitinol Medical Technologies, Inc. include SIMON NITINOL FILTER/STRAIGHT LINE SYSTEM, SIMON NITINOL FILTER, MODIFICATION, SIMON NITINOL FILTER and SIMON NITINOL FILTER SYSTEM.