Imtec Corp.
Imtec Corp. holds FDA 510(k) medical device clearances, first cleared 1991, most recent 2008.
Top product codes for Imtec Corp.
Recent clearances by Imtec Corp.
- K081653 — MDI MII ONE-PIECE IMPLANT, 2.9MM
- K081347 — ILUMA VISION
- K072660 — ENDURE IMPLANT, MODEL 5108, 5111, 5113, 5114
- K053046 — ILUMA ORTHOCAT/DENTALCAT
- K043226 — ENDURE IMPLANT, MODELS 3508, 4308, 3520, 4320
- K042289 — MDI ORTHO
- K033432 — LEXATITE QUICK ACRYLIC
- K031106 — IMTEC SENDAX MDI AND MDI PLUS ENDOSSEOUS IMPLANT, MODELS OB-XX, SH-XX, MOB-22, MSH-XX
- K030243 — ENDURE IMPLANT, MODEL 3508,3511,3514,4308,4311,4314
- K024044 — SABER TECH IMPLANTS SYSTEM
- K023067 — IMTEC SENDAX MDI ORTHO6 AND ORTHO8
- K021437 — SECURE SOFT
- K021586 — SECURE RELINE/PICKUP MATERIAL
- K020396 — BIOCELLECT -PERIO
- K010775 — BIOCELLECT
- K982951 — IMTEC BIOPIN
- K990983 — MODIFICATION TO IMTEC SENDAX MDI
- K974752 — IMTEC/BIOBARRIER MEMBRANE
- K973248 — IMTEC BONE COLLECTOR SYSTEM
- K973180 — IMTEC BONE TAC
- K972240 — IMTEC BIOBARRIER MEMBRANE
- K970841 — IMTEC/TITANIUM MESH
- K950306 — IMTEC BIOBARRIER
- K932168 — HEXLOCK/HEXLOCK SCREW
- K923260 — LAPAROSCOPY SETS, NEEDLE HOLDERS, BLUNT CURVED
- K923259 — LAPAROSCOPY SETS, NEEDLE HOLDERS, BLUNT SHEARS
- K920909 — HEXLOCK SCREW
- K912262 — HEXLOCK
Data sourced from openFDA. This site is unofficial and independent of the FDA.