Data / Medical devices / United States / Medco MFG.
Medco MFG.: FDA-registered device maker in Spring, TX, United States, 2 510(k) clearances
Medco MFG. is registered with the FDA (registration 1649660) in Spring, TX, United States. It lists 9 device types. The FDA files 2 510(k) clearances under its listings, the newest dated March 31, 2017. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 1649660
- FEI number
- 3001451796
- Address
- 8319 THORA No. A1, Spring, TX, United States, 77379
- Owner or operator
- MEDCO MFG. (9031360)
- Roles
- Manufacturer, Repackager or relabeler, Specification developer
- First device listed
- May 6, 2008
- Registered through
- 2026
- Brand names listed
- 2-Hole Wedge, 2-Port Radial, 3 Port 60 Degree Index, 3 Port 60 Degree Index Double, 3 Port Radial, 4 Port 60 Degree Index, 8G, Ab Grater and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Bottle, Collection, Vacuum | KDQ | 2 | Repackager or relabeler | accessdata.fda.gov |
| Cannula, Surgical, General & Plastic Surgery | GEA | 1 | Repackager or relabeler | accessdata.fda.gov |
| Garment, Protective, For Incontinence | EYQ | 1 | Repackager or relabeler | accessdata.fda.gov |
| Instrument, Manual, Surgical, General Use | MDM | 1 | Repackager or relabeler | accessdata.fda.gov |
| Needle, Aspiration And Injection, Reusable | GDM | 1 | Repackager or relabeler | accessdata.fda.gov |
| Pump, Portable, Aspiration (Manual Or Powered) | BTA | 2 | Manufacturer | accessdata.fda.gov |
| Stand, Infusion | FOX | 1 | Specification developer | accessdata.fda.gov |
| System, Suction, Lipoplasty | MUU | 2 | Repackager or relabeler | accessdata.fda.gov |
| Tubing, Noninvasive | GAZ | 2 | Repackager or relabeler | 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 31, 2017 | K170449 | Autoclavable Suction Jar with Luer Lock extension - 250, 500, 1,000, 2,000 and 3,000 ml, Autoclavable Suction Jar without Luer Lock extension - 1,500 and 2,500 ml, Sterile 1,500 and 2,500 Lids with Conical patient connection 6-10 and overflow protection | MUU | Substantially Equivalent | Millennium Medical Technologies, Inc. | accessdata.fda.gov |
| February 12, 1999 | K982371 | MEDCO ASPIRATOR IV | BTA | Substantially Equivalent | Medco Mfg. | accessdata.fda.gov |
Compare with other makers
- All makers of Stand, Infusion
- All makers of Instrument, Manual, Surgical, General Use
- All makers of Bottle, Collection, Vacuum
- All makers of Tubing, Noninvasive
- All makers of Garment, Protective, For Incontinence
- All makers of Pump, Portable, Aspiration (Manual Or Powered)
Updated March 31, 2017. 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.