PERCUSSIONAIRE CORP.

Contract manufacturer · Sandpoint, ID

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

FDA registration

3029845 (openFDA record; or search FDA's registration database)

FEI number

1000524541

Registered for

FDA registration year 2026

Establishment types

Manufacturer; Contract manufacturer; Repackager or relabeler

Owner or operator

PERCUSSIONAIRE CORP. (FDA owner/operator no. 9029650)

Registered address

130 MCGHEE RD STE 109, Sandpoint, ID 83864

Contract listings

1 device listings, 1 product codes, first listed Dec 5, 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.