| Device Type ID | 4359 |
| Device Name | Lens, Contact, (disposable) |
| Regulation Description | Soft (hydrophilic) Contact Lens. |
| Regulation Medical Specialty | Ophthalmic |
| Review Panel | Ophthalmic |
| Premarket Review | Office Of Device Evaluation (ODE) Division Of Ophthalmic And Ear, Nose And Throat Devices (DOED) Contact Lenses And Retinal Devices Branch (CLRD) |
| Submission Type | 510(k) |
| CFR Regulation Number | 886.5925 [🔎] |
| FDA Device Classification | Class 2 Medical Device |
| Product Code | MVN |
| GMP Exempt | No |
| Summary MR | Eligible |
| Implanted Device | No |
| Life Support Device | No |
| Third Party Review | Eligible For Accredited Persons Program |
| Device Type ID | 4359 |
| Device | Lens, Contact, (disposable) |
| Product Code | MVN |
| FDA Device Classification | Class 2 Medical Device |
| Regulation Description | Soft (hydrophilic) Contact Lens. |
| CFR Regulation Number | 886.5925 [🔎] |
| Premarket Reviews | ||
|---|---|---|
| Manufacturer | Decision | |
YUNG SHENG OPTICAL CO., LTD. | ||
SUBSTANTIALLY EQUIVALENT | 2 | |
| Device Problems | |
|---|---|
Adverse Event Without Identified Device Or Use Problem | 44 |
Contact Lens | 4 |
Insufficient Information | 4 |
Torn Material | 2 |
Device Contaminated During Manufacture Or Shipping | 1 |
Appropriate Term/Code Not Available | 1 |
Improper Or Incorrect Procedure Or Method | 1 |
| Total Device Problems | 57 |
| Recalls | |||
|---|---|---|---|
| Manufacturer | Recall Class | Date Posted | |
| 1 | CooperVision Inc. | III | Apr-25-2018 |
| 2 | Johnson & Johnson Vision Care, Inc. | II | Mar-27-2018 |