Megaplast, Inc.
United StatesFDA applicant, unverified
- Devices
- 7
What Megaplast, Inc. makes
Megaplast, Inc. manufactures single-use medical trays and accessories for surgical and procedural settings, including urethral catheterization trays, irrigation trays, and open-heart surgical trays (custom-designed). The company also produces urinary drainage bags, suture removal trays, surgical utility drapes, and ENT syringes for clinical use.
The portfolio includes devices classified as Class I and Class II under FDA regulations, with submissions recorded in the 510(k) clearance registry. Megaplast, Inc. is based in the United States.
Catalogue
Urinary Drainage Bag Ref K820136
Regimes: 510(k) Registry: 510(k)Tray, Catherization, Urethral Ref K810249
Regimes: 510(k) Registry: 510(k)Suture Removal Tray Ref K820423
Regimes: 510(k) Registry: 510(k)Open Heart Tray (Custom Designed) Ref K822158
Regimes: 510(k) Registry: 510(k)Tray, Irrigation Ref K810250
Regimes: 510(k) Registry: 510(k)Surgical Utility Drape Ref K821313
Regimes: 510(k) Registry: 510(k)Syringe, Ent Ref K810251
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Megaplast, Inc. have in the registry?
The registry currently lists 7 devices for Megaplast, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Megaplast, Inc.'s devices?
Among its 7 most recently registered devices, Megaplast, Inc. has devices listed in FDA 510(k) (7 devices).
What risk classes do Megaplast, Inc.'s devices fall under?
Among its 7 most recently registered devices, the classes recorded for Megaplast, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Megaplast, Inc. in the registry?
The most recently registered devices listed for Megaplast, Inc. include URINARY DRAINAGE BAG, TRAY, CATHERIZATION, URETHRAL, SUTURE REMOVAL TRAY and OPEN HEART TRAY (CUSTOM DESIGNED).