CONTAMAC SOLUTIONS, INC.

FDA Device Registration & Listing · Grand Junction, CO, US · Registration 3016114779

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
3016114779
FEI Number
3016114779
Entity Name
CONTAMAC SOLUTIONS, INC.
City/State/Country
Grand Junction, CO, US
Establishment Address
806 Kimball Avenue, Grand Junction, CO 81501, US
Establishment Type(s)
Develop Specifications But Do Not Manufacture At This Facility
Owner / Operator
Contamac Solutions, Inc. (Owner Number: 10061958)
Owner / Operator Contact Address
806 Kimball Avenue, Grand Junction, CO 81501, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
K181566
PMA Number
N/A

All Registered Proprietary Names

Nutrifill

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
MRC Products, Contact Lens Care, Rigid Gas Permeable Ophthalmic Class 2 886.5918 2019-12-06

Official Correspondent

Jessica Labriola

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Contamac Solutions, 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-0030-2022 Contamac Solutions, Inc. 2
Nutrifill Scleral, Hybrid, and Gas Permeable (GP) Lens Insertion Solution, Physiologic Formula, Preservative Free, 35 Single-use 10ml ampoules (360ml), UDI:00850012123002

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3016114779. Last updated year: 2026. Please use registration number 3016114779 when referencing this establishment in official correspondence.
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