Milestones

2016
2016.11 PSA insert- XPE type, XPE LC type and LC type are approved by TFDA, Taiwan.
2016.09 All Poly Tibial Component are approved by TFDA, Taiwan.
2016.04 All Poly Tibial Component are approved by FDA, USA.
2016.08 U2 Knee Modular Disposable trial
2016.04 Revision Femoral Head is approved by TFDA, Taiwan.
2016.04 E-XPE Cemented Cup is approved by TFDA, Taiwan.
2016.04 U-Motion II EXPE Liner is approved by TFDA, Taiwan.
2016.02 U2 Bipolar Implant, 22mm is approved by TFDA, Taiwan.
2016.04 U2 Bipolar Implant, 22mm is approved by FDA, USA.
2016.03 UCP Stem is approved by FDA, USA.
2015
2015.10 U2 femoral head, Ø22mm is approved by TFDA, Taiwan.
2015.10 U2 Knee between size insert is approved by TFDA, Taiwan.
2015.10 U2 Knee between size femoral component is approved by TFDA, Taiwan.
2015.09 U2 Knee between size insert are approved by FDA, USA.
2015.09 U2 Knee between size femoral component is approved by FDA, USA.
2015.08 U-Motion II delta ceramic liner is approved by CFDA, China.
2015.08 U-Motion II delta ceramic head 40 mm is approved by CFDA, China.
2015.08 Femoral head, Ø22mm is approved by CE, Europe.
2015.08 U2 Bipolar Implant, 22 mm I.D. is approved by CE, Europe.
2015.08 U2 All poly tibial component is approved by CE, Europe.
2015.08 U2 Knee between size insert is approved by CE, Europe.
2015.08 U2 Knee between size femoral component is approved by CE, Europe.
2015.08 U2 matrix porous stem is approved by FDA, USA.
2015.04 CENTURY Spinal System II- screw additional products are approved by TFDA, Taiwan.
2015.01 UTF reduced stem #1~#11 is approved by CFDA, China.
2014
2014.12 UCP Cemented Stem is approved by TFDA, Taiwan. 
2014.11 SLIMFIT Anterior Cervical Plate System II is approved by TFDA, Taiwan. 
2014.11 Revision femoral head & 42mm Full XPE cup is approved by CE, Europe. 
2014.11 CENTURY Spinal System II is approved by CE, Europe. 
2014.10 UNIFY Anatomic Plate System is approved by TFDA, Taiwan. 
2014.09 Augment (Tibial: #1~#7; Femoral:#1~#6) is approved by CFDA, China. 
2014.09 U-Motion II (PS Cup & Delta Ceramic Liner) is approved by CFDA, China. 
2014.09 TPS GTF II Stem is approved by TFDA, Taiwan. 
2014.09 Full XPE cup is approved by TFDA, Taiwan. 
2014.09 FENCE Anterior Staple Fixation System is approved by CE, Europe. 
2014.08 2.5mm & 7.5mm Femoral head, is approved by CFDA, China. 
2014.08 U-Motion II (HA+ & PS+ Cup) is approved by CE, Europe. 
2014.08 UCP Stem is approved by CE, Europe. 
2014.06 #7 U2 CR porous coated femoral component is approved by FDA, USA. 
2014.06 #7 U2 CR cemented femoral component is approved by FDA, USA. 
2014.05 Full XPE cup & TPS GTF II Stem is approved by CE, Europe. 
2014.05 U-Motion II PS+ Cup is approved by TFDA, Taiwan. 
2014.04 FENCE Anterior Staple Fixation System is approved by TFDA, Taiwan. 
2014.04 #12-#14 UTF reduced stem is approved by TFDA, Taiwan. 
2014.03 Offset stem adapter is approved by TFDA, Taiwan. 
2014.03 XUC Tibial insert is approved by FDA, USA. 
2014.01 #0 Tibial augment is approved by TFDA, Taiwan. 
2014.01 XUC Tibial insert is approved by TFDA, Taiwan.
2014.01 U2 #7 CMA tibial baseplate, Tibial augment & Tiaial insert is approved by FDA, USA.
2014.01 U2 #0 & #7 CMA tibial baseplate & Tibial insert is approved by TFDA, Taiwan.
2013
2013.12 U-Motion II acetabular system is awarded the 10th National Innovation Award. 
2013.12 Biolox Option is approved by TFDA, Taiwan.
2013.12 XUC/ UTF stem-reduced #12,13,14/ GTF II is approved by CE, Europe.
2013.09 GTF II stem is approved by TFDA, Taiwan.
2013.09 U-Motion II PS+ Cup is approved by FDA, USA.
2013.08 CMA baseplate is approved by CE, Europe.
2013.08 Delta Head is approved by CFDA, China.
2013.08 UTF stem-reduced #12,13,14 is approved by FDA, USA.
2013.06 PSA Augment extension line is approved by TFDA, Taiwan.
2013.05 Biolox Option, # 0 & 7 Tibial augment, Offset stem adapter is approved by CE, Europe.
2013.05 UTF stem-reduced is approved by FDA, USA.
2013.03 UTF stem and Cage System are approved by SFDA, China.
2013.03 Femoral Heads (2.5 and 7.5 mm Neck Length) are approved by TFDA, Taiwan.
2013.03 UTF stem-reduced is approved by TFDA, Taiwan.
2013.02 U-Motion II acetabular system is approved by FDA, USA.
2013.02 U-Motion II acetabular system is approved by TFDA, Taiwan.
2013.02 PSA Augment extension line is approved by FDA, USA.
2013.01 Century II spinal system is approved by TFDA, Taiwan.
2012
2012.08 U2 Knee XPE Insert, Patella was approved in China. 
2012.08 UOC USA Inc. was established in Irvine, California. 
2012.08 U2 PSA Revision Knee with excellent quality obtained "SNQ" National Quality certification Medal. 
2012.08 U2 Revision Hip Stem obtained certification in China. 
2012.07 U2 Plasma spray acetabular cup was approved by US FDA. (K121777) 
2012.05 Bipolar II was approved by SFDA, China.
2012.05 U-motion Ceramic Acetabular System was approved by SFDA, China.
2012.05 U2 Knee, PS type, #7 was approved by US FDA. (K120507)
2012.03 United Compression Intramedullary Pinning was approved by DOH, Taiwan (#003619)