Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3006638854

FEI Number

3004158845

Entity Name

LERNAPHARM INC.

City/State/Country

SAINT-LAURENT Quebec, CA

Establishment Address

2323 HALPERN, SAINT-LAURENT Quebec H4S1S3, CA

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

LERNAPHARM INC. (Owner Number: 9104462)

Owner / Operator Contact Address

2323 HALPERN, --, SAINT LAURENT, QUEBEC, CA-NOTA H4S 1S3, CA

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

LERNA Lubricating Jelly

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
KMJ	Lubricant, Patient	General Hospital	Class 1	880.6375	2024-11-08
NEC	Bandage, Liquid, Skin Protectant	General Hospital	Class 1	880.5090	2016-11-17

Official Correspondent

No official correspondent registered.

US Agent Details

Micah Reynolds Business: Ramboll US Consulting, Inc. Email: mreynolds@ramboll.com Phone: (703) 5162349

Related Public Records

Same Entity

LERNAPHARM 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
K820587	Abco Dealers, Inc.	WET PACK LINE OF PRODUCTS	1982-03-26

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3006638854. Last updated year: 2026. Please use registration number 3006638854 when referencing this establishment in official correspondence.