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Data / Medical devices / United States / Post Medical, Inc.

Post Medical, Inc.: FDA-registered device maker in Alpharetta, GA, United States, 2 510(k) clearances

Post Medical, Inc. is registered with the FDA (registration 1034525) in Alpharetta, GA, United States. It lists 1 device type. The FDA files 2 510(k) clearances under its listings, the newest dated April 21, 1999. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number
1034525
FEI number
1000016009
Address
555 N Point Ctr E, Alpharetta, GA, United States, 30022
Owner or operator
Post Medical, Inc. (10035763)
Roles
Manufacturer, Repackager or relabeler, Specification developer
First device listed
March 23, 2011
Registered through
2026
Brand names listed
Sharps Containment System, Voyager

Devices it lists

DeviceProduct codeClassRoleSource
Needle, Hypodermic, Single LumenFMI2Manufacturer, Repackager or relabeler, Specification 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
April 21, 1999K990371DIABETIC NEEDLE DISPOSAL, MODEL # PMSM - 950FMISubstantially EquivalentPost Medical, Inc.accessdata.fda.gov
April 29, 1994K925816SHARPS CONTAINMENT SYSTEMFMISubstantially EquivalentPost Medical, Inc.accessdata.fda.gov

Compare with other makers

Updated April 21, 1999. 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.