MedtechSourcebook

K Line Florida

Contract manufacturer · West Palm Beach, FL

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

FDA registration
3044462786 (openFDA record; or search FDA's registration database)
FEI number
3044462786
Registered for
FDA registration year 2026
Establishment types
Manufacturer; Contract manufacturer
Owner or operator
K LINE EUROPE GMBH (FDA owner/operator no. 10079939)
Registered address
1860 Okeechobee Road, Suite 402, West Palm Beach, FL 33409
Contract listings
2 device listings, 1 product codes, first listed Apr 6, 2022
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
NXCAligner, SequentialClass IIDentalContract manufacturingApr 6, 2022