DIVA INTERNATIONAL, INC.

FDA Device Registration & Listing · KITCHENER Ontario, CA · Registration 3005113602

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
3005113602
FEI Number
3005113602
Entity Name
DIVA INTERNATIONAL, INC.
City/State/Country
KITCHENER Ontario, CA
Establishment Address
222 McIntyre Dr, KITCHENER Ontario N2R 1E8, CA
Establishment Type(s)
Foreign Private Label Distributor,Repack or Relabel Medical Device
Owner / Operator
Diva International Inc (Owner Number: 9072098)
Owner / Operator Contact Address
222 McIntyre Drive, Kitchener, CA-ON N2R 1E8, CA
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

The Lubricator DivaCup Model 2 DivaCup Model 1 DivaCup Model 0 Diva Disc Diva PL Model A Diva PL Model B Diva Reusable Underwear Diva Biome Balancer Applicator Diva Cramp Care Patch

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
NUC Lubricant, Personal Obstetrics/Gynecology Class 2 884.5300 2025-03-14
HHE Cup, Menstrual Obstetrics/Gynecology Class 2 884.5400 2008-02-07
NUQ Pad, Menstrual, Reusable Obstetrics/Gynecology Class 1 884.5435 2023-08-11
HGD Applicator, Vaginal Obstetrics/Gynecology Class 1 884.4520 2026-02-05
IMD Pack, Hot Or Cold, Disposable Physical Medicine Class 1 890.5710 2025-09-16

Official Correspondent

No official correspondent registered.

US Agent Details

David Lennarz Business: Registrar Corp Email: david.lennarz@registrarcorp.com Phone: (757) 2240177

Related Public Records

Same Entity

Diva International 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
K050212 Qualis, Inc. PERSONAL WARMING JELLY 2005-03-17
K880871 John Wagner Associates, Inc. GRABBER WARM PACK/MINI MINI HEATER/FOOT HEATER 1988-05-20

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
Z-0505-2022 Philips North America Llc 1
Infa-Therm Transport Mattress, Reference Number 989805616831 1015
Z-0506-2022 Philips North America Llc 1
Infant Heel Warmers w/strap, Reference # 989805603201 1223

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3005113602. Last updated year: 2026. Please use registration number 3005113602 when referencing this establishment in official correspondence.
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