Data / Medical devices / United States / 3CPM Company., INC.
3CPM Company., INC.: FDA-registered device maker in Sparks Glencoe, MD, United States, 1 510(k) clearance
3CPM Company., INC. is registered with the FDA (registration 2954356) in Sparks Glencoe, MD, United States. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated August 20, 1999. Registered through 2026. FDA data exported November 3, 2026.
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- FDA registration number
- 2954356
- FEI number
- 3002900388
- Address
- 954 Ridgebrook Road, STE 220, Sparks Glencoe, MD, United States, 21152
- Owner or operator
- 3CPM Company., INC. (9039837)
- Roles
- Manufacturer
- First device listed
- December 6, 2007
- Registered through
- 2026
- Brand names listed
- 3CPM Electrogastrography/Electroviscerography System
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| System, Electrogastrography (Egg) | MYE | 2 | Manufacturer | 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 |
|---|---|---|---|---|---|---|
| August 20, 1999 | DEN990005 | THE 3PM EGG MACHINE | MYE | Unknown | 3pm Co., Inc. | accessdata.fda.gov |
Compare with other makers
Updated August 20, 1999. 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.