510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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VENTUREMED GROUP, Inc

Plymouth, MN, US

VENTUREMED GROUP, Inc appears in FDA device records in Plymouth, MN. FDA records list 2 510(k) clearances between and , no PMA records and one registered establishment. 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
2
PMA records
0
Recall records
0
Registered establishments
1

510(k) clearance history

FDA records hold 2 510(k) clearances for VENTUREMED GROUP, Inc between 2016 and 2020. The busiest year on record is 2016, with 1. The most recent is 2020, with 1.

Clearances by year, as a table
510(k) clearance decisions for VENTUREMED GROUP, Inc, by decision year
YearClearances
20161
20201
510(k) clearances on record, most recent first
K numberDeviceProduct codeDecisionDecision date
K202187FLEX Vessel Prep SystemPNOSubstantially Equivalent
K152789FLEX SCORING CATHETERPNOSubstantially Equivalent

Registered establishments

FDA registered establishments for VENTUREMED GROUP, Inc, with the product codes listed at each
RegistrationFEIEstablishmentAddressRegistration expiresProduct codes listed
30126966533012696653VENTUREMED GROUP, Inc2800 Campus Dr., Plymouth, MN 55441 US2026

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