Data / Medical devices / United States / Milkmate
Milkmate: FDA-registered device maker in New York, NY, United States, 1 510(k) clearance
Milkmate is registered with the FDA (registration 3027115730) in New York, NY, United States. It lists 2 device types. The FDA files 1 510(k) clearance under its listings, the newest dated March 16, 2023. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3027115730
- Address
- 521 5th Ave Fl 18 Ste 1808, New York, NY, United States, 10175
- Owner or operator
- MilkMate (10087772)
- Roles
- Complaint file establishment
- First device listed
- April 6, 2023
- Registered through
- 2026
- Brand names listed
- MilkMate Breast Pump, MilkMate Insert
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Pump, Breast, Powered | HGX | 2 | Complaint file establishment | accessdata.fda.gov |
| Shield, Nipple | HFS | 1 | Complaint file establishment | accessdata.fda.gov |
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| March 16, 2023 | K223084 | MilkMate Breast Pump | HGX | Substantially Equivalent | Milkmate Products, Inc. | accessdata.fda.gov |
Compare with other makers
Updated March 16, 2023. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.