HAMILTON THORNE, Inc.
Registration 1221433FEI 1221433Beverly, MA
Owner/operator: Hamilton Thorne, Inc.
- Complaint File Establishment per 21 CFR 820.198
- Develop Specifications But Do Not Manufacture At This Facility
- Manufacture Medical Device
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
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- Dec 1Our pay-by date30 days left
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- FDA fee, FY2027
- $13,785
- Our pay-by suggestion
- Dec 1
- Listed devices
- 31
- Added, last 12 months
- 0
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 31
| Code | Device | Class | Regulation | Premarket |
|---|---|---|---|---|
| MQG | Geri Connect Server (including software)Accessory, Assisted Reproduction | Class 2 | 21 CFR 884.6120 | K180188 |
| MQG | Geri DishAccessory, Assisted Reproduction | Class 2 | 21 CFR 884.6120 | K180304 |
| PUB | FERTY Syringe PlusAccessory, Assisted Reproduction, Exempt | Class 2 | 21 CFR 884.6120 | — |
| MQF | #2000 Semtrac Set 5Catheter, Assisted Reproduction | Class 2 | 21 CFR 884.6110 | K013536 |
| MQF | #4220 IUICatheter, Assisted Reproduction | Class 2 | 21 CFR 884.6110 | K013501 |
| GKL | CEROSCounter, Cell, Automated (Particle Counter) | Class 2 | 21 CFR 864.5200 | K920719 |
| GKZ | LensHooke C-KUP Liquefaction Test CupCounter, Differential Cell | Class 2 | 21 CFR 864.5220 | K180343 |
| MQK | Geri DishLabware, Assisted Reproduction | Class 2 | 21 CFR 884.6160 | K180304 |
| PUD | 4-Chamber Analysis SlideLabware, Assisted Reproduction, Exempt | Class 2 | 21 CFR 884.6160 | — |
| NRF | accu-beadsMaterial, Quality Control, Semen Analysis | Class 2 | 21 CFR 864.8625 | — |
| MQL | GM501 Wash with Phenolred and Gentamicin (PRG)Media, Reproductive | Class 2 | 21 CFR 884.6180 | K192503 |
| MQL | GM501 WashMedia, Reproductive | Class 2 | 21 CFR 884.6180 | K190383 |
and 19 more on your full dossier
What changed
Nothing added in the last twelve months, and no change seen on the record yet.