PENTA LATEX LLP

FDA Device Registration & Listing · Haridwar Uttarakhand, IN · Registration 3013408180

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
3013408180
FEI Number
3013408180
Entity Name
PENTA LATEX LLP
City/State/Country
Haridwar Uttarakhand, IN
Establishment Address
Plot No. 49 & 50,, Sector-2, SIIDCUL, Ranipur, Haridwar Uttarakhand 249403, IN
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner / Operator
Penta Latex LLP (Owner Number: 10052829)
Owner / Operator Contact Address
Plot No. 49 & 50,, Sector-2, SIIDCUL, Ranipur, Haridwar, IN-UT 249403, IN
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

No proprietary names listed under this establishment.

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
HIS Condom Obstetrics/Gynecology Class 2 884.5300 2016-10-10

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

Penta Latex LLP
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 3013408180. Last updated year: 2026. Please use registration number 3013408180 when referencing this establishment in official correspondence.
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