Reprolife America, LLC

FDA Device Registration & Listing · Kingwood, TX, US · Registration 3018010054

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
3018010054
FEI Number
3018010054
Entity Name
Reprolife America, LLC
City/State/Country
Kingwood, TX, US
Establishment Address
22751 Professional Dr Ste 220, Kingwood, TX 77339, US
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Experimental Culture Media Productions and Consignment, LLC (Owner Number: 10092108)
Owner / Operator Contact Address
22751 Professional Dr, Ste 220, Kingwood, TX 77339, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
K233846
PMA Number
N/A

All Registered Proprietary Names

ECMPC, LLC Reprolife America, LLC Cryotec America, LLC

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
MQL Media, Reproductive Obstetrics/Gynecology Class 2 884.6180 2024-12-05

Official Correspondent

Mindy Blackston

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Experimental Culture Media Productions and Consignment, LLC
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
K011481 Conception Technologies 10% PVP; 10% PVP IN EBSS SOLUTION 2001-07-02

Similar Registrations

Registration Number Establishment Name Location
2031824 Vitrolife Inc. San Diego, CA, US
3014295858 COOPER MEDICAL, SRL La Garita Alajuela, CR
3014755376 CooperSurgical Distribution B.V. Herten Limburg, NL
3036725842 GYNOTEC B.V. Malden Gelderland, NL
3004048494 ORIGIO A/S Ballerup Hovedstaden, DK
Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3018010054. Last updated year: 2026. Please use registration number 3018010054 when referencing this establishment in official correspondence.
Legal Disclaimer: AvaSpecs is not affiliated with the FDA or any government agency and does not provide medical, legal, regulatory, safety, approval, clearance, effectiveness, endorsement, or compliance advice. This index page is built using public record archives and does not represent an official regulatory determination.
Account Required Full available specs will require a free AvaSpecs account.