Data / Medical devices / United States / United Products & Instruments, Inc.
United Products & Instruments, Inc.: FDA-registered device maker in Dayton, NJ, United States, 1 510(k) clearance
United Products & Instruments, Inc. is registered with the FDA (registration 2249760) in Dayton, NJ, United States. It lists 8 device types. The FDA files 1 510(k) clearance under its listings, the newest dated November 15, 2007. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 2249760
- FEI number
- 3000200590
- Address
- 182 Ridge Rd Ste E, Dayton, NJ, United States, 08810
- Owner or operator
- UNITED PRODUCTS & INSTRUMENTS, INC. (9043530)
- Roles
- Repackager or relabeler
- First device listed
- November 19, 2007
- Registered through
- 2026
- Brand names listed
- Colpo-Master Colposcope, Dermascout, G300 Series Microscopes, G500 Series Microscopes, L-BC Series Differential Counters, L-CU Series Laboratory Incubators, M250 Series Microscopes, M280 Series Microscopes and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Bath, Incubators/Water, All | JTQ | 1 | Repackager or relabeler | accessdata.fda.gov |
| Centrifuge, Hematocrit | GKG | 2 | Repackager or relabeler | accessdata.fda.gov |
| Centrifuges (Micro, Ultra, Refrigerated) For Clinical Use | JQC | 1 | Repackager or relabeler | accessdata.fda.gov |
| Colposcope (And Colpomicroscope) | HEX | 2 | Repackager or relabeler | accessdata.fda.gov |
| Equipment, Laboratory, General Purpose, Labeled Or Promoted For A Specific Medical Use | LXG | 1 | Repackager or relabeler | accessdata.fda.gov |
| Hand-Tally, Differential | GKM | 1 | Repackager or relabeler | accessdata.fda.gov |
| Light, Microscope | IBJ | 1 | Repackager or relabeler | accessdata.fda.gov |
| Mixer, Blood Tube | GLE | 1 | 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 |
|---|---|---|---|---|---|---|
| November 15, 2007 | K073053 | COLPO-MASTER | HEX | Substantially Equivalent | United Products & Instruments, Inc. | accessdata.fda.gov |
Compare with other makers
- All makers of Equipment, Laboratory, General Purpose, Labeled Or Promoted For A Specific Medical Use
- All makers of Centrifuge, Hematocrit
- All makers of Centrifuges (Micro, Ultra, Refrigerated) For Clinical Use
- All makers of Mixer, Blood Tube
- All makers of Light, Microscope
Updated November 15, 2007. 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.