Planet Innovation Products, Inc.
Registration 2022994FEI 2022994IRVINE, CA
Owner/operator: Planet Innovation Products, Inc.
- Manufacture Medical Device for Another Party (Contract Manufacturer)
Renewal due by December 31, 2026
Registered through 2026. Renew between October 1 and December 31, 2026, to stay registered for 2027.
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The 2026 window
- Oct 1Window opens91 days left
- Nov 3Where you stand58 days left
- Dec 1Our pay-by date30 days left
- Dec 15Two weeks left16 days left
- Dec 23Holiday week8 days left
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- Dec 31Window closes0 days left
- FDA fee, FY2027
- $13,785
- Our pay-by suggestion
- Dec 1
- Listed devices
- 9
- Added, last 12 months
- 1
FDA sets who pays the fee and who may qualify for a waiver; its fee page says so. The fee is paid only on FDA’s own fee site. Never through us. FDA’s fee page
The steps, in order
Pay FDA's annual feeYou
Order and pay the FY2027 establishment fee on FDA's Device Facility User Fee site. FDA emails you a PIN when you order.
FDA: registration and listing payment processWait for the payment confirmation numberYou
FDA emails a Payment Confirmation Number (PCN) once the payment processes, which FDA says typically takes several days. That is why we suggest paying by December 1.
FDA: registration and listing payment processRenew the registration in FDA's systemYou
Sign in to FDA's Unified Registration and Listing System (FURLS), complete the annual registration and apply your PIN and PCN. FDA does not count the registration as complete until both are applied.
FDA: device registration and listingReview every listingYou
In the same window, review each listing on file and report any changes, deletions and new listings. Your Listing Review Sheet puts every listing on one page.
FDA: device registration and listing
Every listed device 9
| Code | Device | Class | Regulation | Premarket |
|---|---|---|---|---|
| FRN | KLEIN TOUCH PUMP AND DISPOSABLE TUBING SETPump, Infusion | Class 2 | 21 CFR 880.5725 | — |
| FRN | KLEIN SURGICAL INFILTRATION PUMP, MODEL KIP-IIPump, Infusion | Class 2 | 21 CFR 880.5725 | — |
| QDZ | Alethia CMV DNA Amplification Assay, Alethia CMV External Control KitQualitative Cytomegalovirus Nucleic Acid-Based Detection Device For Congenital Cytomegalovirus Infection | Class 2 | 21 CFR 866.3181 | — |
| OOI | Fast PCR Instrument; Fast PCR Mini Respiratory Panel; Fast PCR Mini Respiratory Panel Negative External Control; Fast PCReal Time Nucleic Acid Amplification SystemAdded Jul 30, 2026 | Class 2 | 21 CFR 862.2570 | — |
| QPB | HK LIPOSUCTION ASPIRATOR, MODEL AP-III & AP230-IIISystem, Suction, Lipoplasty For Removal | Class 2 | 21 CFR 878.5040 | — |
| DHB | CLA ALLERGEN-SPECIFIC IGE ASSAY-LATEX ALLERGEN (K82)System, Test, Radioallergosorbent (Rast) Immunological | Class 2 | 21 CFR 866.5750 | — |
| GQG | Sofia2Antigen, Cf (Including Cf Controls), Respiratory Syncytial Virus | Class 1 | 21 CFR 866.3480 | — |
| OMN | ILLUMIGENE C. DIFFICILE, ILLUMIPRO-10 AND ILLUMIGENE C. DIFFICILE EXTERNAL CONTROL KIT, MODELS 280050, 610172, 279920C. Difficile Nucleic Acid Amplification Test Assay | Class 1 | 21 CFR 866.2660 | — |
| KHO | Sofia2Fluorometer, For Clinical Use | Class 1 | 21 CFR 862.2560 | — |
What changed
- Jul 30, 2026Listing added: OOI — Fast PCR Instrument; Fast PCR Mini Respiratory Panel; Fast PCR Mini Respiratory Panel Negative External Control; Fast PC