Aptyx - Charlotte
Registration 3011324393FEI 3011324393Charlotte, NC
Owner/operator: Aptyx
- Manufacture Device in the United States for Export Only
- 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
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- FDA fee, FY2027
- $13,785
- Our pay-by suggestion
- Dec 1
- Listed devices
- 11
- 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 11
| Code | Device | Class | Regulation | Premarket |
|---|---|---|---|---|
| SEQ | EndoForce Connector for Endovascular Venous AnastomosisCovered Stent Vascular Connector, Hemodialysis Access Circuit | Class 3 | — | — |
| QSK | AMDS Hybrid ProsthesisHybrid Stent Graft, Thoracic Aortic Lesion Treatment | Class 3 | — | — |
| MIH | Ascyrus Medical Dissection Stent (AMDS)System, Endovascular Graft, Aortic Aneurysm Treatment | Class 3 | — | — |
| MAI | Ziptek, ZipSFastener, Fixation, Biodegradable, Soft Tissue | Class 2 | 21 CFR 888.3030 | — |
| MBI | Ziptek, ZipSFastener, Fixation, Nondegradable, Soft Tissue | Class 2 | 21 CFR 888.3040 | — |
| MQV | POROUS BIOLOGIC SCAFFOLDFiller, Bone Void, Calcium Compound | Class 2 | 21 CFR 888.3045 | — |
| BYZ | HBC; HBP; Hensler Bone Collector, Hensler Bone PressTrap, Sterile Specimen | Class 2 | 21 CFR 880.6740 | — |
| KNT | CORGRIP* SR NG/NI Tube Retention SystemTubes, Gastrointestinal (And Accessories) | Class 2 | 21 CFR 876.5980 | — |
| QXR | Vaginal Hydrogel Packing SystemVaginal Hydrogel Packing System | Class 2 | 21 CFR 892.5735 | — |
| KGS | Ziptek, ZipSRetention Device, Suture | Class 1 | 21 CFR 878.4930 | — |
| PFE | Endobarrier Gastrointestinal LinerGastrointestinal Liner SystemAdded Mar 10, 2026 | Not classified | — | — |
What changed
- Mar 10, 2026Listing added: PFE — Endobarrier Gastrointestinal Liner