Data / Medical devices / Pakistan / Clearpath Orthodontics
Clearpath Orthodontics: FDA-registered device maker in Lahore Punjab, Pakistan, 3 510(k) clearances
Clearpath Orthodontics is registered with the FDA (registration 3009157552) in Lahore Punjab, Pakistan. It lists 2 device types. The FDA files 3 510(k) clearances under its listings, the newest dated January 5, 2021. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3009157552
- Address
- 6-N Johar Town, Lahore Punjab, Pakistan, 54700
- Owner or operator
- Clearpath Orthodontics (10051683)
- Roles
- Exporter to the US, Manufacturer
- First device listed
- April 20, 2016
- Registered through
- 2026
- Brand names listed
- ClearPath Aligner, Clearpath Aligner, Defence Dental Center
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Aligner, Sequential | NXC | 2 | Exporter to the US, Manufacturer | accessdata.fda.gov |
| Plier, Orthodontic | JEX | 1 | 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 |
|---|---|---|---|---|---|---|
| January 5, 2021 | K202857 | ClearPath Aligner | NXC | Substantially Equivalent | Clearpath Orthodontics, Ltd. | accessdata.fda.gov |
| July 6, 2017 | K162609 | ClearPath Aligner | NXC | Substantially Equivalent | Clearpath Orthodontics, Ltd. | accessdata.fda.gov |
| November 1, 2013 | K123514 | CLEARPATH ALIGNER | NXC | Substantially Equivalent | Qserve America, Inc. | accessdata.fda.gov |
Compare with other makers
Updated January 5, 2021. 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.