POST MEDICAL, INC.

FDA Device Registration & Listing · Alpharetta, GA, US · Registration 1034525

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
1034525
FEI Number
1000016009
Entity Name
POST MEDICAL, INC.
City/State/Country
Alpharetta, GA, US
Establishment Address
555 N Point Ctr E, Alpharetta, GA 30022, US
Establishment Type(s)
Repack or Relabel Medical Device,Develop Specifications But Do Not Manufacture At This Facility,Manufacture Medical Device
Owner / Operator
Post Medical, Inc. (Owner Number: 10035763)
Owner / Operator Contact Address
555 North Point Center E, Alpharetta, GA 30022, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
K990371
PMA Number
N/A

All Registered Proprietary Names

Sharps Containment System Voyager

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
FMI Needle, Hypodermic, Single Lumen General Hospital Class 2 880.5570 2011-03-23
FMI Needle, Hypodermic, Single Lumen General Hospital Class 2 880.5570 2011-03-23

Official Correspondent

Tony Lair

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Post Medical, Inc.
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Related 510(k) Records

510(k) Number Applicant Device Name Decision Date
K812404 Nu Tech Medical Systems BUTTERFLY NEEDLE ASSEMBLY 1981-09-09

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
Z-0002-2022 Bard Peripheral Vascular Inc 2
REF TIN3015, 15G x 79 mm Bone Marrow Aspiration/Intraosseous Infusion Needle, For Single Use Only, Sterile EO, UDI: 10885403043796

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 1034525. Last updated year: 2026. Please use registration number 1034525 when referencing this establishment in official correspondence.
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