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Iop, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
9
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K090078KERASYS BIOENGINEERED LAMELLAR PATCH GRAFTMay 8, 2009
K062252MOLTENO3September 27, 2006
K053622SURGISIS OCULAR GRAFTMarch 15, 2006
K010852OSMED TISSUE EXPANDERAugust 13, 2001
K003646SUTUREGROOVE WEIGHT SIZING SETFebruary 22, 2001
K994289SUTUREGROOVEApril 17, 2000
K972143MOA BONE / M-SPHEREOctober 16, 1997
K902489MODIFIED MOLTENO(TM) IMPLANTSAugust 14, 1990
K890598MOLTENO IMPLANTFebruary 27, 1989