NORDENT MFG., INC.
Registration 1419489FEI 1419489ELK GROVE VILLAGE, IL
Owner/operator: NORDENT MFG., INC.
- Develop Specifications But Do Not Manufacture At This Facility
- Manufacture Medical Device
- Manufacture Medical Device for Another Party (Contract Manufacturer)
- Repack or Relabel Medical Device
Renewal due by December 31, 2026
Registered through 2026. Renew between October 1 and December 31, 2026, to stay registered for 2027.
90days left in the window
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
- Dec 29Two days left2 days left
- Dec 31Window closes0 days left
- FDA fee, FY2027
- $13,785
- Our pay-by suggestion
- Dec 1
- Listed devices
- 71
- 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 71
| Code | Device | Class | Regulation | Premarket |
|---|---|---|---|---|
| EBZ | I LED, I LED II, O-LIGHT, O-LIGHT IIActivator, Ultraviolet, For Polymerization | Class 2 | 21 CFR 872.6070 | K080025 |
| DZI | AI SURGERYDrill, Bone, Powered | Class 2 | 21 CFR 872.4120 | K111290 |
| ILY | D-Laser 16, D-Laser Blue, LX 16, LX16 PlusLamp, Infrared, Therapeutic Heating | Class 2 | 21 CFR 890.5500 | K210367 |
| NVK | D-Laser 16, D-Laser Blue, LX 16, LX16 PlusLaser, Dental, Soft Tissue | Class 2 | 21 CFR 878.4810 | K210367 |
| GEX | D-Laser 16, D-Laser Blue, LX 16, LX16 PlusPowered Laser Surgical Instrument | Class 2 | 21 CFR 878.4810 | K210367 |
| ELC | D600 LEDScaler, Ultrasonic | Class 2 | 21 CFR 872.4850 | K053555 |
| ELC | AI SURGERYScaler, Ultrasonic | Class 2 | 21 CFR 872.4850 | K111290 |
| ELC | ultrasonic scalerScaler, Ultrasonic | Class 2 | 21 CFR 872.4850 | K210832 |
| EJI | Syringe, CartridgeSyringe, Cartridge | Class 2 | 21 CFR 872.6770 | — |
| EHD | Ai Ray LiteUnit, X-Ray, Extraoral With Timer | Class 2 | 21 CFR 872.1800 | K222569 |
| EKJ | NORDENT AMALGAM BURNISHERSBurnisher, Operative | Class 1 | 21 CFR 872.4565 | — |
| KTZ | CalipersCaliper | Class 1 | 21 CFR 888.4150 | — |
and 59 more on your full dossier
What changed
- Apr 20, 2026Listing added: DZP — Instrument, Diamond, Dental