U&I Corp.
12 FDA 510(k) clearances · Manufacturer
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| Record | Firm | Date |
|---|---|---|
| VELOXTM INTERBODY FUSION SYSTEM (K140864) | U&I Corp. | 2014-07-22 |
| ASPIRON ACP SYSTEM (K140234) | U&I Corp. | 2014-06-02 |
| VELOFIXTM INTERBODY FUSION SYSTEM (K132926) | U&I Corp. | 2014-03-05 |
| DYNA LOCKING ANKLE NAIL (K120419) | U&I Corp. | 2012-05-21 |
| DYNA LOCKING CANNULATED SCREW (K112240) | U&I Corp. | 2012-01-04 |
| OPTIGEN TOTAL KNEE SYSTEM (K102367) | U&I Corp. | 2010-12-08 |
| DYNA LOCKING TROCHANTERIC NAIL, MODEL NG0820 (K093707) | U&I Corp. | 2010-06-23 |
| DYNA LOCKING IM NAIL (K092771) | U&I Corp. | 2009-12-02 |
| PERFIX SPINAL SYSTEM, MODEL SNA4530-9610, SNM4530-9610, SN3020 (TOTAL: 549) (K091725) | U&I Corp. | 2009-11-09 |
| MAXIMA ANTERIOR CERVICAL PLATE SYSTEM (K061002) | U&I Corp. | 2006-11-15 |
| OPTIMA SPINAL SYSTEM (K051971) | U&I Corp. | 2005-08-04 |
| MODIFICATION TO GLOBAL SPINAL FIXATION SYSTEM (K042928) | U&I Corp. | 2005-02-17 |
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Every clearance here is in the API, with alerts when new ones post.