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Sprintray Inc.

Los Angeles, CA, US

SPRINTRAY INC. appears in FDA device records in Los Angeles, CA. FDA records list 9 510(k) clearances between and , no PMA records and 2 registered establishments. As of , FDA records show no recalls for this company, and at least one establishment registration is current.

FDA records held for this company

510(k) clearances
9
PMA records
0
Recall records
0
Registered establishments
2

510(k) clearance history

FDA records hold 9 510(k) clearances for Sprintray Inc. between 2021 and 2026. The busiest year on record is 2022, with 3. The most recent is 2026, with 1.

Clearances by year, as a table
510(k) clearance decisions for Sprintray Inc., by decision year
YearClearances
20211
20223
20231
20242
20251
20261
510(k) clearances on record, most recent first
K numberDeviceProduct codeDecisionDecision date
K260661Midas RestoreEBFSubstantially Equivalent
K250617Apex FlexEBISubstantially Equivalent
K242559Digital TempEBGSubstantially Equivalent
K242277Crown HTEBFSubstantially Equivalent
K230445OnX ToughEBISubstantially Equivalent
K222623Digital CrownEBFSubstantially Equivalent
K221678SprintRay High Impact Denture BaseEBISubstantially Equivalent
K220979SprintRay Denture BaseEBISubstantially Equivalent
K212448NightGuard FlexMQCSubstantially Equivalent

Registered establishments

FDA registered establishments for Sprintray Inc., with the product codes listed at each
RegistrationFEIEstablishmentAddressRegistration expiresProduct codes listed
30142896653014289665SPRINTRAY INC.2710, 2705 Media Center Dr Ste 100A, Los Angeles, CA 90065 US2026and 1 more, listed in full below
30247496973024749697SPRINTRAY INC.17601 Sampson Ln., Huntington Beach, CA 92647 US2026and 1 more, listed in full below

Registration numbers link to the FDA registration and listing record for that establishment.

FDA product codes

Recall records

No recall records for this company in the ingested FDA data.

Verification record

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Data as of , FDA export datePage updated Source: openFDA, public domain