GENESIS INDUSTRIES, INC.

FDA Device Registration & Listing · ELMWOOD, WI, US · Registration 2183741

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
2183741
FEI Number
2183741
Entity Name
GENESIS INDUSTRIES, INC.
City/State/Country
ELMWOOD, WI, US
Establishment Address
601 PRO-JECT DR., ELMWOOD, WI 54740, US
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
GENESIS INDUSTRIES, INC. (Owner Number: 2183741)
Owner / Operator Contact Address
303 SOUTH MCKAY AVE.,, P.O. BOX 39, SPRING VALLEY, WI 54767, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

NOVO VIVO ASPIRATION INJECTION NEEDLES

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 1988-04-01

Official Correspondent

No official correspondent registered.

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

GENESIS INDUSTRIES, INC.
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Other Registrations for Same Entity

Registration Number Establishment Name Location
3003697955 MAI/GENESIS ELMWOOD, WI, US

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 2183741. Last updated year: 2026. Please use registration number 2183741 when referencing this establishment in official correspondence.
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