Dental Device Guide
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Not currently registered with FDA under this name

Stryker Cmf

Kalamazoo, MI, United States. Named as applicant on 2 dental 510(k) clearances between 2006 and 2007. No establishment is registered with FDA under this exact name today.

Device types listed
0
Brands and models
0
510(k) clearances
22006–2007
Markets registered in
1United States
Establishments
0—
2006: 12007: 1200020102020

510(k) clearances per year, 2000–2026

510(k) clearances

Clearances on which FDA names Stryker Cmf as the applicant.

Decided510(k)DeviceDevice type
10 Aug 2007K071628STRYKER EXTERNAL FIXATION SYSTEMMQN External Mandibular Fixator and/or Distractor
19 Apr 2006K060750STRYKER INJECTABLE CEMENTNEA Nose and Throat Ear Cement

Sources

FDA 510(k) premarket notification file. FDA data as of 2 Nov 2026; snapshot 12 Nov 2026. The location shown is the address on FDA's record of the most recent filing, which can be a US agent.