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Dyansys, Inc.

Orinda, CA, US

Dyansys, Inc. appears in FDA device records in Orinda, CA. FDA records list 15 510(k) clearances between and , no PMA records and no registered establishments. As of , FDA records show no recalls for this company.

FDA records held for this company

510(k) clearances
15
PMA records
0
Recall records
0
Registered establishments
0

510(k) clearance history

FDA records hold 15 510(k) clearances for Dyansys, Inc. between 2007 and 2022. The busiest year on record is 2022, with 4. The most recent is 2022, with 4.

Clearances by year, as a table
510(k) clearance decisions for Dyansys, Inc., by decision year
YearClearances
20072
20081
20092
20151
20171
20181
20201
20212
20224
510(k) clearances on record, most recent first
K numberDeviceProduct codeDecisionDecision date
K221425Primary ReliefNHISubstantially Equivalent
K221231Drug Relief v1PZRSubstantially Equivalent
K220397ANSiStim-PPNHISubstantially Equivalent
K213188Primary ReliefNHISubstantially Equivalent
K212859First ReliefNHISubstantially Equivalent
K211971Drug Relief v1PZRSubstantially Equivalent
K202940First Relief v1QHHSubstantially Equivalent
K173861Drug ReliefPZRSubstantially Equivalent
K170391ANSiStim-PPBWKSubstantially Equivalent
K141168ANSISTIMBWKSubstantially Equivalent
K091397ECSCOPE 200DPSSubstantially Equivalent
K091358ECSCOPE 100DPSSubstantially Equivalent
K080036PORTABLE ECSCOPE 12IDPSSubstantially Equivalent
K071168THE PORTABLE ANSISCOPEDPSSubstantially Equivalent
K072353PORTABLE ECSCOPEDPSSubstantially Equivalent

Registered establishments

No FDA establishment registrations recorded against this company.

FDA product codes

Recall records

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

Verification record

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What MDM checks, and what it does not

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