MQU
4 FDA 510(k) clearances · Product code
FDA profile
- Official device name
- Ocular Peg
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 886.3320
- Medical specialty
- Ophthalmic
- Flags
- Implant
Export predicate table (CSV) Shareable report ◉ Watch exports: 3 free/month · reports & watching: free
| Record | Firm | Date |
|---|---|---|
| PERRY-KOLBERG (PK) HA-COATED TITANIUM SLEEVE (K000151) | Integrated Orbital Implants, Inc. | 2000-04-10 |
| TITANIUM PEG SYSTEM (K980822) | Fci Ophthalmics, Inc. | 1998-07-09 |
| PERRY-KOLBERG (PK) TITANIUM MOTILITY/SUPPORT SYSTEM (K974203) | Integrated Orbital Implants, Inc. | 1998-02-04 |
| MEDPOR OCULAR SCREW AND ACCEOSSORIES (K971583) | Porex Technologies Corp. | 1997-06-30 |
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Every clearance here is in the API, with alerts when new ones post.