MAUDE GROUP, INC.

FDA Device Registration & Listing · New York, NY, US · Registration 3013986076

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
3013986076
FEI Number
3013986076
Entity Name
MAUDE GROUP, INC.
City/State/Country
New York, NY, US
Establishment Address
161 Water Street, #2025, New York, NY 10038, US
Establishment Type(s)
Repack or Relabel Medical Device
Owner / Operator
Maude Group, Inc. (Owner Number: 10055751)
Owner / Operator Contact Address
161 Water Street, #2025, New York, NY 10038, US
Initial Importer Flag
Y
Expiration Date (Year)
2026
510(k) Number
K012964
PMA Number
N/A

All Registered Proprietary Names

Maude Latex Condom Rise Maude Rise Plus

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
HIS Condom Obstetrics/Gynecology Class 2 884.5300 2017-11-07
HIS Condom Obstetrics/Gynecology Class 2 884.5300 2021-04-15

Official Correspondent

No official correspondent registered.

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Maude Group, Inc.
View consolidated registration, premarket clearance, and recall records for this applicant.
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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3013986076. Last updated year: 2026. Please use registration number 3013986076 when referencing this establishment in official correspondence.
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