Reflow Medical

Contract manufacturer · Lake Forest, CA

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

FDA registration

3027058844 (openFDA record; or search FDA's registration database)

FEI number

3027058844

Registered for

FDA registration year 2026

Establishment types

Manufacturer; Contract manufacturer; Repackager or relabeler

Owner or operator

Reflow Medical (FDA owner/operator no. 10034685)

Registered address

20532 Crescent Bay Dr. Suite 100, Lake Forest, CA 92630

Contract listings

1 device listings, 1 product codes, first listed Nov 20, 2025

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.