Data / Medical devices / United States / Miele Inc.
Miele Inc.: FDA-registered device maker in Princeton, NJ, United States, 1 510(k) clearance
Miele Inc. is registered with the FDA (registration 2248632) in Princeton, NJ, United States. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated November 12, 2003. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 2248632
- FEI number
- 1000526822
- Address
- 9 Independence Way, Princeton, NJ, United States, 08540
- Owner or operator
- Miele Inc. (10025486)
- Roles
- Complaint file establishment
- First device listed
- April 17, 2008
- Registered through
- 2026
- Brand names listed
- Miele
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Device, Pasteurization, Hot Water | LDS | 2 | 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 |
|---|---|---|---|---|---|---|
| November 12, 2003 | K031799 | MIELE DENTAL THERMAL DISINFECTOR, MODEL G7881 | LDS | Substantially Equivalent | Miele, Inc. | accessdata.fda.gov |
Compare with other makers
Updated November 12, 2003. 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.