Dymax, Corp.
Country not established FDA establishment FEI 3013041594
- Devices
- 7
- Registrations
- FDA
- FDA recalls
- 0
Catalogue
Dymax Personal Scanner Ref K862127
510(k) 510(k)Site-Rite 3 Ultrasound System Ref K993624
510(k) 510(k)Plus 1 Ref K850478
510(k) 510(k)Siterite Needle Guide (Modified) Ref K931403
510(k) 510(k)Siterite Needle Guide Ref K903158
510(k) 510(k)Dymax Endovaginal Biopsy Guide Ref K894415
510(k) 510(k)Site-Rite Iv Ultrasound System Ref K032135
510(k) 510(k)
Company details
- FDA FEI number
- 3013041594
- Address
- 141 Zehner School Rd, Zelienople, PA, 16063
Frequently asked questions
How many devices does Dymax, Corp. have in the registry?
The registry currently lists 7 devices for Dymax, Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Dymax, Corp.'s devices?
Among its 7 most recently registered devices, Dymax, Corp. has devices listed in FDA 510(k) (7 devices).
What risk classes do Dymax, Corp.'s devices fall under?
Among its 7 most recently registered devices, the classes recorded for Dymax, Corp.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Dymax, Corp. in the registry?
The most recently registered devices listed for Dymax, Corp. include DYMAX PERSONAL SCANNER, SITE-RITE 3 ULTRASOUND SYSTEM, PLUS 1 and SITERITE NEEDLE GUIDE (MODIFIED).