VIBRALUNG, INC.

FDA Device Registration & Listing · Parker, CO, US · Registration 3007858792

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
3007858792
FEI Number
3007858792
Entity Name
VIBRALUNG, INC.
City/State/Country
Parker, CO, US
Establishment Address
11990 Meadowood Lane, Parker, CO 80138, US
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
VibraLung, Inc. (Owner Number: 10084462)
Owner / Operator Contact Address
11990 Meadowood Lane, Parker, CO 80138, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
K133057
PMA Number
N/A

All Registered Proprietary Names

Vibralung® Patient Change Kit Vibralung® Mask Interface Kit-Adult with Aerosol Delivery System Vibralung® Acoustical Percussor Vibralung® Treatment Control Unit Vibralung® Mask Interface Kit-Pediatric w/Aerosol Delivery System Vibralung® Trach Interface Kit with Aerosol Delivery System Vibralung® Patient Kit Vibralung® HHT Hanger Vibralung® Full User Kit/Travel Bag

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
SDT Intra-Pulmonary Percussive Vibration (Ipv) Devices Anesthesiology Class 2 868.5665 2022-02-24

Official Correspondent

Lucille Hughes

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

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

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3007858792. Last updated year: 2026. Please use registration number 3007858792 when referencing this establishment in official correspondence.
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