Contamac Solutions, Inc.
Grand Junction, CO, US
CONTAMAC SOLUTIONS, INC. appears in FDA device records in Grand Junction, CO. FDA records list no 510(k) clearances, no PMA records and one registered establishment. As of , FDA records show 2 recalls for this company, and at least one establishment registration is current.
FDA records held for this company
510(k) clearance history
No 510(k) clearance records for this company in the ingested FDA data.
No 510(k) clearance records in the ingested FDA data.
Registered establishments
| Registration | FEI | Establishment | Address | Registration expires | Product codes listed |
|---|---|---|---|---|---|
| 3016114779 | 3016114779 | CONTAMAC SOLUTIONS, INC. | 806 Kimball Avenue, Grand Junction, CO 81501 US | 2026 | No device listings on this registration |
Registration numbers link to the FDA registration and listing record for that establishment.
FDA product codes
No FDA product codes recorded against this company.
Recall records
| Recall | Product | Reason | Classification | Initiated | Status |
|---|---|---|---|---|---|
| Z-1956-2025 | Contamac, Nutrifill Physiologic formula, Contact Lens Insertion solution | Contact lens insertion solution may lack sterility. | Class II | Open, Classified | |
| Z-0030-2022 | Nutrifill Scleral, Hybrid, and Gas Permeable (GP) Lens Insertion Solution, Physiologic Formula, Preservative Free, 35 Single-use 10ml ampoules (360ml), UDI:00850012123002 | Contact lens solution may contain foreign material | Class II | Terminated |
Verification record
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Data as of , FDA export datePage updated Source: openFDA, public domain