INTEROJO, Inc.
INTEROJO, Inc. appears in FDA public data with 0 recalls, 4 510(k) clearances, 2 FDA inspections, and 1 compliance action on record. Its most recent 510(k) clearance was granted on May 29, 2026.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 4
- Inspections
- 2
- Compliance Actions
- 1
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K260507 | Interojo 45 (inofilcon A) Soft (Hydrophilic) Silicone Hydrogel Contact Lens with GrabSoo Plus | May 29, 2026 |
| K221517 | POLYVUE (polymacon) Soft (hydrophilic) Contact Lens, POLYVUE COLOR (polymacon) Soft (hydrophilic) Co | October 4, 2022 |
| K153766 | Clalen 54 (hioxifilcon D) Soft (hydrophilic) Contact Lens for Daily Wear, Clalen 58 (hioxifilcon A) | April 8, 2016 |
| K142766 | I-55 (methafilcon A) Soft (hydrophilic) Contact Lenses for Daily Wear | March 12, 2015 |