Aukland Medical Plastics, Inc.
United StatesFDA applicant, unverified
- Devices
- 3
What Aukland Medical Plastics, Inc. makes
Aukland Medical Plastics, Inc. manufactures single-use medical devices, including the AUKULYTE—a disposable fluid management system—and the AUKUSLEEVE, a protective sleeve for medical tubing. The company also produces POST-MYDS(TM), a post-mastectomy drainage system designed for surgical use.
These devices are classified as Class I under FDA regulations and are listed via 510(k) clearance. The company operates from the United States.
Catalogue
Aukulyte Ref K953610
Regimes: 510(k) Registry: 510(k)Aukusleeve Ref K930094
Regimes: 510(k) Registry: 510(k)Post-Myds(Tm) Ref K930840
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Aukland Medical Plastics, Inc. have in the registry?
The registry currently lists 3 devices for Aukland Medical Plastics, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Aukland Medical Plastics, Inc.'s devices?
Among its 3 most recently registered devices, Aukland Medical Plastics, Inc. has devices listed in FDA 510(k) (3 devices).
What risk classes do Aukland Medical Plastics, Inc.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Aukland Medical Plastics, Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Aukland Medical Plastics, Inc. in the registry?
The most recently registered devices listed for Aukland Medical Plastics, Inc. include AUKULYTE, AUKUSLEEVE and POST-MYDS(TM).