MedtechSourcebook

Cicor Ohio, Solon

Contract manufacturer ยท Solon, OH

FDA-registered (openFDA, export of Oct 21, 2026) ISO 13485: not verified

FDA registration
3010129044 (openFDA record; or search FDA's registration database)
FEI number
3010129044
Registered for
FDA registration year 2026
Establishment types
Contract manufacturer
Owner or operator
Cicor Ohio, Solon (FDA owner/operator no. 10043204)
Registered address
29200 Fountain Pkwy, Solon, OH 44139
Contract listings
2 device listings, 1 product codes, first listed Jul 24, 2024
Certification
Not verified. We have no certification data for this facility yet.

Devices listed as contract work

Each row is an FDA product code this facility lists under its contract establishment type, with the date of its earliest such listing.

Product codeDevice (FDA name)ClassCategoryRoleFirst listed
OLOOrthopedic Stereotaxic InstrumentClass IINeurologyContract manufacturingJul 24, 2024