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Data / Medical devices / United States / Evenflo Feeding Incorporated

Evenflo Feeding Incorporated: FDA-registered device maker in West Chester, OH, United States, 3 510(k) clearances

Evenflo Feeding Incorporated is registered with the FDA (registration 3009826814) in West Chester, OH, United States. It lists 3 device types. The FDA files 3 510(k) clearances under its listings, the newest dated November 3, 2023. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number
3009826814
Address
8200 Beckett Park Dr Ste 111, West Chester, OH, United States, 45069
Owner or operator
Evenflo Feeding, Inc. (10041987)
Roles
Specification developer
First device listed
September 27, 2012
Registered through
2026
Brand names listed
EVENFLO ADVANCED MANUAL BREAST PUMP, EVENFLO ADVANCED SINGLE ELECTRIC BREAST PUMP, EVENFLO POCKET PORTABLE DOUBLE ELECTRIC BREAST PUMP, Evenflo Advanced Disposable Nursing Pads, Evenflo Advanced Double Electric Breast Pump, Evenflo Advanced Nursing Pads, Evenflo Basics Nursing Pads, Evenflo Manual Breast Pump

Devices it lists

DeviceProduct codeClassRoleSource
Fiber, Medical, AbsorbentFRL1Specification developeraccessdata.fda.gov
Pump, Breast, Non-PoweredHGY1Specification developeraccessdata.fda.gov
Pump, Breast, PoweredHGX2Specification developeraccessdata.fda.gov

510(k) clearances

The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.

Decided510(k) numberDeviceProduct codeDecisionApplicantSource
November 3, 2023K230481Evenflo Premium Double Electric Breast Pump (Model 4018)HGXSubstantially EquivalentEvenflo Feeding, Inc.accessdata.fda.gov
June 18, 2013K131153EVENFLO ADVANCED DOUBLE ELECTRIC BREAST PUMPHGXSubstantially EquivalentEvenflo Feeding Incorporatedaccessdata.fda.gov
December 22, 2010K102600SIMPLYGO BREAST PUMPHGXSubstantially EquivalentEvenflo Company, Inc.accessdata.fda.gov

Compare with other makers

Updated November 3, 2023. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.