Pneumeric, Inc.

FDA Device Registration & Listing · Luverne, MN, US · Registration 3020664622

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
3020664622
FEI Number
3020664622
Entity Name
Pneumeric, Inc.
City/State/Country
Luverne, MN, US
Establishment Address
604 Britz Dr, c/o Johnathon Aho, Luverne, MN 56156, US
Establishment Type(s)
Develop Specifications But Do Not Manufacture At This Facility
Owner / Operator
Pneumeric, Inc. (Owner Number: 10082878)
Owner / Operator Contact Address
604 Britz Dr, Luverne, MN 56156, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
PMA Number
N/A

All Registered Proprietary Names

CapnoSpot™ Pneumothorax Decompression Indicator

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
GAA Needle, Aspiration And Injection, Disposable General, Plastic Surgery Class 1 878.4800 2023-06-14

Official Correspondent

Robert McLain

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Pneumeric, 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
K781371 Ferris Mfg. Corp. BONE MARROW ASPIRATION KIT 1978-09-20

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
Z-0017-2023 Hobbs Medical, Inc. 1
Hobbs Transbronchial Aspiration Needle and Vacu-lok Aspirating Syringe Catalog Number: 4620
Z-0018-2023 Hobbs Medical, Inc. 1
Hobbs Transbronchial Aspiration Needle Catalog Number: 4621
Z-0023-2011 Becton Dickinson & Company 1
BD 30G1/2 PrecisionGlide Needle;Catalog/Lot Number: 305106. Needles are intended for use in aspiration and injection of medications.

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3020664622. Last updated year: 2026. Please use registration number 3020664622 when referencing this establishment in official correspondence.
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