MedtechSourcebook

Planet Innovation Products, Inc.

Contract manufacturer ยท Irvine, CA

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

2012Product codes first listed, by year (tallest: 3)2026
FDA registration
2022994 (openFDA record; or search FDA's registration database)
FEI number
2022994
Registered for
FDA registration year 2026
Establishment types
Contract manufacturer
Owner or operator
Planet Innovation Products, Inc. (FDA owner/operator no. 9063957)
Registered address
80 Technology Drive, Irvine, CA 92618
Contract listings
8 device listings, 8 product codes, first listed Dec 26, 2012
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
DHBSystem, Test, Radioallergosorbent (Rast) ImmunologicalClass IIImmunologyContract manufacturingDec 26, 2012
FRNPump, InfusionClass IIGeneral hospitalContract manufacturingDec 26, 2012
GQGAntigen, Cf (Including Cf Controls), Respiratory Syncytial VirusClass IMicrobiologyContract manufacturingNov 27, 2023
KHOFluorometer, For Clinical UseClass IClinical chemistryContract manufacturingNov 27, 2023
OMNC. Difficile Nucleic Acid Amplification Test AssayClass IMicrobiologyContract manufacturingDec 26, 2012
OOIReal Time Nucleic Acid Amplification SystemClass IIClinical chemistryContract manufacturingJul 30, 2026
QDZQualitative Cytomegalovirus Nucleic Acid-Based Detection Device For Congenital Cytomegalovirus InfectionClass IIMicrobiologyContract manufacturingJun 17, 2021
QPBSystem, Suction, Lipoplasty For RemovalClass IIGeneral and plastic surgeryContract manufacturingJun 17, 2021