B&B MOLDED PRODUCTS

FDA Device Registration & Listing · Defiance, OH, US · Registration 3012736230

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
3012736230
FEI Number
3012736230
Entity Name
B&B MOLDED PRODUCTS
City/State/Country
Defiance, OH, US
Establishment Address
1250 Ottawa Ave., Defiance, OH 43512, US
Establishment Type(s)
Repack or Relabel Medical Device
Owner / Operator
B&B Molded Products (Owner Number: 10052524)
Owner / Operator Contact Address
1250 Ottawa Ave., Defiance, OH 43512, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Naturelle

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
HHD Pad, Menstrual, Unscented Obstetrics/Gynecology Class 1 884.5435 2016-08-10

Official Correspondent

Neal Carter

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

B&B Molded Products
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
K823241 Kimberly-Clark Corp. NEW FREEDOM THIN UNSCENTED MAXI PADS 1982-12-28

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3012736230. Last updated year: 2026. Please use registration number 3012736230 when referencing this establishment in official correspondence.
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