Data / Medical devices / Philippines / Mesco, Inc.
Mesco, Inc.: FDA-registered device maker in Pasig City National Capital Region, Philippines, 1 510(k) clearance
Mesco, Inc. is registered with the FDA (registration 3009662565) in Pasig City National Capital Region, Philippines. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated March 12, 2004. Registered through 2027. FDA data exported November 2, 2026.
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- FDA registration number
- 3009662565
- Address
- Reliance cor. Brixton Sts., Kapitoyo, Pasig City National Capital Region, Philippines, 1603
- Owner or operator
- MESCO, INC. (10057990)
- Roles
- Contract manufacturer, Exporter to the US
- First device listed
- June 30, 2018
- Registered through
- 2027
- Brand names listed
- Bone Plates, Volar Bearing Plates
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Plate, Fixation, Bone | HRS | 2 | Contract manufacturer, Exporter to the US | 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 12, 2004 | K040112 | TRIMED BEARING PLATE; TRIMED VOLAR BEARING PLATE | HRS | Substantially Equivalent | Tri-Med, Inc. | accessdata.fda.gov |
Compare with other makers
Updated March 12, 2004. 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.