Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3005367964

FEI Number

3005367964

Entity Name

MOLECULAR PRODUCTS INC

City/State/Country

Louisville, CO, US

Establishment Address

633 CTC Boulevard, Suite 200, Louisville, CO 80027, US

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

Molecular Products Inc (Owner Number: 10035691)

Owner / Operator Contact Address

633 CTC Boulevard, Suite 200, Louisville, CO 80027, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Sodasorb LF Sofnolime Sodasorb HMED CO2 Absorber DYNJAACO2LF CO2 Absorber DYNJAACO2BAG Aria CO2 Absorber DYNJAACO2CAN CO2 Absorber DYNJAACO2DISC Sodasorb HMED Sofnolime Sodasorb LF

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
BSF	Absorber, Carbon-Dioxide	Anesthesiology	Class 1	868.5310	2020-06-25
CBL	Absorbent, Carbon-Dioxide	Anesthesiology	Class 1	868.5300	2011-03-15

Official Correspondent

Ruben Colmenares

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Molecular Products Inc

View consolidated registration, premarket clearance, and recall records for this applicant.

View Entity Profile →

Related Recall Records

Recall ID	Recalling Firm	Recall Class	Product Description
Z-0006-2008	Datex Ohmeda, Inc	1	GE Disposable Multi Absorber Canister used with EZchange Module for the Aisys, Avance, Aespire Anesthesia systems. The EZchange Module is an optional accessory for these anesthesia systems.

Similar Registrations

Registration Number	Establishment Name	Location
8010042	MAQUET CRITICAL CARE AB	SOLNA Stockholm, SE
3002807637	MOLECULAR PRODUCTS LTD	HARLOW Essex, GB
3016904853	SAINT JONES MANAGEMENT LP EOOD	Sofia Sofia-Grad, BG
1066427	INFINIUM MEDICAL, INC.	Largo, FL, US
3034669683	HUZHOU JUNDA INDUSTRY CO., LTD.	Anji Zhejiang, CN

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3005367964. Last updated year: 2026. Please use registration number 3005367964 when referencing this establishment in official correspondence.