Allied Vision Group Inc
Fort Lauderdale, FL, US
ALLIED VISION GROUP, INC. appears in FDA device records in Fort Lauderdale, FL. FDA records list no 510(k) clearances, no PMA records and one registered establishment. As of , FDA records show one recall 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 |
|---|---|---|---|---|---|
| 2247018 | 1000122287 | ALLIED VISION GROUP, INC. | 5350 NW 35th Ave, FORT LAUDERDALE, FL 33309 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-1821-2020 | Alcon Air Optix Night & Day Aqua (lotrafilcon A), breathable contact lenses, PWR - 1.50 BC 8.6 DIA 13.8, Rx, Sterile. The firm name on the label is Alcon Laboratories, Inc., Fort Worth, TX. | Potentially counterfeit products in/and counterfeit packaging were imported to the U.S. | Class II | Completed |
Verification record
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Data as of , FDA export datePage updated Source: openFDA, public domain