FDA 510(k) Applications Submitted by IOP, INC.

FDA 510(k) Number Submission Date Device Name Applicant
K090078 01/12/2009 KERASYS BIOENGINEERED LAMELLAR PATCH GRAFT IOP, INC.
K010852 03/21/2001 OSMED TISSUE EXPANDER IOP, INC.
K972143 06/06/1997 MOA BONE / M-SPHERE IOP, INC.
K062252 08/03/2006 MOLTENO3 IOP, INC.
K003646 11/27/2000 SUTUREGROOVE WEIGHT SIZING SET IOP, INC.
K994289 12/21/1999 SUTUREGROOVE IOP, INC.
K053622 12/28/2005 SURGISIS OCULAR GRAFT IOP, INC.


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