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EM Innovations Inc

Galloway, OH, US

EM INNOVATIONS, INC. appears in FDA device records in Galloway, OH. FDA records list one 510(k) clearance, no PMA records and one registered establishment. As of , FDA records show one recall for this company, and at least one establishment registration is current.

FDA records held for this company

510(k) clearances
1
PMA records
0
Recall records
1
Registered establishments
1

510(k) clearance history

FDA records hold 1 510(k) clearance for EM Innovations Inc in 1994.

Clearances by year, as a table
510(k) clearance decisions for EM Innovations Inc, by decision year
YearClearances
19941
510(k) clearances on record, most recent first
K numberDeviceProduct codeDecisionDecision date
K935407STICKITFMISubstantially Equivalent

Registered establishments

FDA registered establishments for EM Innovations Inc, with the product codes listed at each
RegistrationFEIEstablishmentAddressRegistration expiresProduct codes listed
15299901000515375EM INNOVATIONS, INC.6106 BAUSCH ROAD, GALLOWAY, OH 43119 US2026

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

FDA product codes

Recall records

Device recall records naming this company, most recent first
RecallProductReasonClassificationInitiatedStatus
Z-0056-2007Model EMI 82691, Stic Kit Needle Containment Device. These devices are packaged 60 per case. Stick-on label on device and User Instruction sheet are attached to the case with a rubber band.The firm failed to include User Instructions with the Stic Kit Needle Containment Device, Model EMI 82691, which they shipped to distributor/customers.Terminated

Verification record

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