Home › Device types › MQU
Ocular Peg
FDA product code MQU · Class 2 · Ophthalmic
6
Registered devices
1
Adverse events
1
Recalls
4
510(k) clearances
Devices with this code
P-K Titanium Motility Peg System — INTEGRATED ORBITAL IMPLANTS INCP-K Titanium Motility Peg System — INTEGRATED ORBITAL IMPLANTS INCP-K Titanium Motility Peg System — INTEGRATED ORBITAL IMPLANTS INCP-K Titanium Motility Peg System — INTEGRATED ORBITAL IMPLANTS INCP-K Titanium Motility Peg System — INTEGRATED ORBITAL IMPLANTS INCP-K Titanium Motility Peg System — INTEGRATED ORBITAL IMPLANTS INC
Recent recalls
| Date | Firm | Reason |
|---|---|---|
| 2006-12-20 | Integrated Orbital Implants Inc | The threads on the threaded sleeve were manufactured with left-handed threads, requiring a modification to the surgical technique for proper insertion. Failure |
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