Sprintray, Inc.
Active in EUDAMEDUnited Statesfrom SRN EUDAMED FDA SRN US-MF-000036081 FEI 3014289665
- Devices
- 215
- Registrations
- EUDAMEDFDA
- FDA recalls
- 0
At a glance
EU certificates
1 of 1 in force.
Market reach
- European Union
- EUDAMED actor, 1 certificate
- United States
- FDA FEI
- Authorised rep.
- SprintRay Europe GmbHDE
What Sprintray, Inc. makes
Sprintray, Inc. manufactures dental appliance fabrication materials, specifically resins used for producing dental prosthetics and surgical guides. Their product line includes surgical guides, crowns in various shades and formulations (such as HT A1, Bleach, B1, C2, D2), digital temporaries, and high-impact and standard denture teeth in shades A1, A2, and A3, all supplied in single-unit capsule or multi-pack formats.
These devices are classified as Class I, Class II, and Class IIa medical devices and are listed in regulatory databases including EUDAMED, the FDA 510(k) database, and the FDA UDI system. The company is based in the United States.
Catalogue
Search and filter all 215 devicesShowing 1-50 of 215
Company details
- EUDAMED SRN
- US-MF-000036081
- FDA FEI number
- 3014289665
- DUNS number
- 063005260
- EUDAMED status
- Active
- EUDAMED registered name
- Sprintray Inc.
- Registered address
- 2710, Media Center Dr Suite, 90065, Los Angeles, United States
- info@sprintray.com
- Phone
- 800-914-8004
- PRRC contact
- Sara Moghtadernejad
EUDAMED certificates
1 certificate1 valid, 0 expiredMDR 1next expiry 29 Apr 2030
DQS Medizinprodukte GmbH 0297 1 certificate
- 1000318152 Active
Quality management system EU MDR
- Issued
- 17 Aug 2026
- Expires
- 29 Apr 2030
- Reason
- Add device or group
Frequently asked questions
How many devices does Sprintray, Inc. have in the registry?
The registry currently lists 215 devices for Sprintray, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Sprintray, Inc.'s devices?
Among its 50 most recently registered devices, Sprintray, Inc. has devices listed in EUDAMED (28 devices) and FDA GUDID (44 devices). A device can be listed in more than one registry, so these counts overlap.
What risk classes do Sprintray, Inc.'s devices fall under?
Among its 50 most recently registered devices, the classes recorded for Sprintray, Inc.'s devices are Class I, Class IIa and Class II. Each device page shows its own class and authorisation.
What EUDAMED certificates are recorded for Sprintray, Inc.?
EUDAMED lists 1 certificate for Sprintray, Inc. (quality management system) under MDR. The most recent was issued on 17 Aug 2026.
What are the newest devices from Sprintray, Inc. in the registry?
The most recently registered devices listed for Sprintray, Inc. include OnX Tough 2 - A2 - Multi-Unit Capsule 1-Pack, Digital Temp - B1 - Multi-Unit Capsule 1-Pack, OnX Tough 2 - B1 - Multi-Unit Capsule 3-Pack and OnX Tough 2 - Hollywood White - Multi-Unit Capsule 1-Pack.