Sylvan Corp.
United Statesfrom the FDA registration address FDA FEI 1000121549
- Devices
- 1
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
What Sylvan Corp. makes
Sylvan Corp. makes the Sylvan PediaScan 200 Transilluminator, a device used for transillumination in pediatric examinations.
The Sylvan PediaScan 200 Transilluminator is classified as a Class I medical device and is listed in the FDA 510(k) registry. Sylvan Corp. is based in the United States.
Catalogue
Sylvan Pediascan 200 Transilluminator Ref K901309
Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 1000121549
- Address
- 612 Cedar St., Irwin, PA, 15642
Frequently asked questions
How many devices does Sylvan Corp. have in the registry?
The registry currently lists 1 device for Sylvan Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Sylvan Corp.'s devices?
Among its 1 most recently registered device, Sylvan Corp. has devices listed in FDA 510(k) (1 device).
What risk classes do Sylvan Corp.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Sylvan Corp.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Sylvan Corp. in the registry?
The most recently registered devices listed for Sylvan Corp. include SYLVAN PEDIASCAN 200 TRANSILLUMINATOR.