M&M PURE AIR SYSTEMS LLC

FDA Device Registration & Listing · Lewes, DE, US · Registration 3025583702

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
3025583702
FEI Number
3025583702
Entity Name
M&M PURE AIR SYSTEMS LLC
City/State/Country
Lewes, DE, US
Establishment Address
16192 Coastal Hwy, Lewes, DE 19958, US
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
M&M PURE AIR SYSTEMS LLC (Owner Number: 10086952)
Owner / Operator Contact Address
16192 Coastal Hwy, Lewes, DE 19958, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

WoodyKnows Mouth Tape; WoodyKnows Lip Tape WoodyKnows Nasal Spray / Steam Inhaler WoodyKnows Nasal Oil Diffuser WoodyKnows Nasclear Nasal Filter; WoodyKnows Allerscreen Nasal Filter; WoodyKnows Enhancer Nasal Filter WoodyKnows Ultra-Thin Nasal Dilator; WoodyKnows Ultra-Breathable Nasal Filter; WoodyKnows Enhancer Nasal Dilator; WoodyKnows Racer Nasal Dilator; WoodyKnows Super-Defense Nasal Filter; WoodyKnows Dynamic Nasal Dilator; WoodyKnows Breasmooth Nasal Dilator; WoodyKnows Super-Support Nasal Dilator WoodyKnows Side-Sleeping Backpack

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
KGX Tape And Bandage, Adhesive General Hospital Class 1 880.5240 2026-05-22
KCO Nasal Spray, Ent Delivery Ear, Nose, Throat Class 1 874.5220 2023-08-25
LWF Dilator, Nasal Ear, Nose, Throat Class 1 874.3900 2022-12-26
MRI Orthosis, Truncal/Orthosis, Limb Physical Medicine Class 1 890.3490 2022-12-26

Official Correspondent

Lei Wang

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

M&M PURE AIR SYSTEMS LLC
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
K843874 Beiersdorf, Inc. LEUKOPOR SURGICAL TAPE 1985-02-21
K915446 Sun Glitz Corp. STRETCH WRAP 1992-05-06
K833120 Acme United Corp. ONE TIME COMPOUND BENZOIN TINCTURE- 1983-12-29
K870091 Avery Intl. IV SECUREMENT DEVICE USING PCCE THERMO. FILM 1987-02-04

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3025583702. Last updated year: 2026. Please use registration number 3025583702 when referencing this establishment in official correspondence.
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