Sun Glitz Corp.
United Statesfrom the FDA registration address FDA FEI 1000115088
- Devices
- 1
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
What Sun Glitz Corp. makes
Sun Glitz Corp. manufactures stretch wrap, a flexible plastic film designed for securing and protecting items in packaging applications.
The company’s products are classified as Class I medical devices under FDA regulations and are listed via 510(k) clearance. The manufacturer is based in the United States.
Catalogue
Stretch Wrap Ref K915446
Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 1000115088
- Address
- 111 SOUTH MCVICKER DR., ENERGY, IL, 62933
Frequently asked questions
How many devices does Sun Glitz Corp. have in the registry?
The registry currently lists 1 device for Sun Glitz Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Sun Glitz Corp.'s devices?
Among its 1 most recently registered device, Sun Glitz Corp. has devices listed in FDA 510(k) (1 device).
What risk classes do Sun Glitz Corp.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Sun Glitz Corp.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Sun Glitz Corp. in the registry?
The most recently registered devices listed for Sun Glitz Corp. include STRETCH WRAP.