RECE INTERNATIONAL CORP.
Registration 3003965134FEI 3003965134Miami, FL
Owner/operator: RECE INTERNATIONAL CORP.
- 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
- 117
- Added, last 12 months
- 2
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 117
| Code | Device | Class | Regulation | Premarket |
|---|---|---|---|---|
| FER | Well Care (Wuhan) Medical Technology Co. Ltd.Anoscope And Accessories | Class 2 | 21 CFR 876.1500 | K230439 |
| DXQ | Blood Pressure CuffCardiovascular | Class 2 | 21 CFR 870.1120 | K190902 |
| EZL | VIAMED FOLEY CATHETERCatheter, Retention Type, Balloon | Class 2 | 21 CFR 876.5130 | K082815 |
| MMK | Viamed Hypodermic Single Lumen NeedleContainer, Sharps | Class 2 | 21 CFR 880.5570 | K082042 |
| FLL | Continuous Measurement ThermometerGeneral Hospital | Class 2 | 21 CFR 880.2910 | K092447 |
| PUI | Viamed Surgical DrapeDrape, Surgical, Exempt | Class 2 | 21 CFR 878.4370 | — |
| DRX | VIAMED ECG ELECTRODESElectrode, Electrocardiograph | Class 2 | 21 CFR 870.2360 | K041954 |
| PIF | ViaMed Enteral Feeding Gravity Set Bag Connector EnfitGastrointestinal Tubes With Enteral Specific ConnectorsAdded Mar 16, 2026 | Class 2 | 21 CFR 876.5980 | K240052 |
| FHN | Well Care (Wuhan) Medical Technology Co. Ltd.Ligator, Hemorrhoidal | Class 2 | 21 CFR 876.4400 | — |
| DQA | VIAMED OXIMETEROximeter | Class 2 | 21 CFR 870.2700 | K082641 |
| LHI | ViaMed BURETTE SET 150MLSet, I.V. Fluid TransferAdded Mar 16, 2026 | Class 2 | 21 CFR 880.5440 | K120424 |
| FMK | VIAMED BLOOD LANCETSingle Use Only Blood Lancet With An Integral Sharps Injury Prevention Feature | Class 2 | 21 CFR 878.4850 | — |
and 105 more on your full dossier
What changed
- Mar 16, 2026Listing added: PIF — ViaMed Enteral Feeding Gravity Set Bag Connector Enfit (K240052)
- Mar 16, 2026Listing added: LHI — ViaMed BURETTE SET 150ML (K120424)