Data / Medical devices / United States / Orthopli Corp.
Orthopli Corp.: FDA-registered device maker in Philadelphia, PA, United States, 1 510(k) clearance
Orthopli Corp. is registered with the FDA (registration 2518634) in Philadelphia, PA, United States. It lists 7 device types. The FDA files 1 510(k) clearance under its listings, the newest dated August 2, 2010. Registered through 2027. FDA data exported November 2, 2026.
SpecStream is the live web data engine for teams and agents. It reads the FDA registration and listing, 510(k), PMA, recall and enforcement files from openFDA every week, and this page is that reading, joined by the FDA's own numbers. Ask for the makers of any device type in any country and new clearances, approvals and recalls arrive in your sheet, CRM, Slack or agent as the FDA publishes them.
- FDA registration number
- 2518634
- Address
- 10061 Sandmeyer LN., Philadelphia, PA, United States, 19116
- Owner or operator
- ORTHOPLI CORP. (2518634)
- Roles
- Manufacturer, Repackager or relabeler, Specification developer
- First device listed
- August 9, 2000
- Registered through
- 2027
- Brand names listed
- ORTHOPLI CORPORATION, Orthopli Corporation, VARIOUS ORTHODONTIC PLIERS
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Accessories, Retractor, Dental | EIF | 1 | Repackager or relabeler, Specification developer | accessdata.fda.gov |
| Epilator, High Frequency, Tweezer-Type | KCX | 1 | Manufacturer | accessdata.fda.gov |
| Handle, Instrument, Dental | EJB | 1 | Manufacturer | accessdata.fda.gov |
| Instrument, Manual, Surgical, General Use | MDM | 1 | Manufacturer | accessdata.fda.gov |
| Plier, Orthodontic | JEX | 1 | Manufacturer | accessdata.fda.gov |
| Sterilization Wrap Containers, Trays, Cassettes & Other Accessories | KCT | 2 | Specification developer | accessdata.fda.gov |
| Tray, Impression, Preformed | EHY | 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 |
|---|---|---|---|---|---|---|
| August 2, 2010 | K101653 | MILTEX THOMPSON CASSETTES; MILTEX SURGICAL CASSETTES | KCT | Substantially Equivalent | Miltex, Inc. | accessdata.fda.gov |
Compare with other makers
- All makers of Epilator, High Frequency, Tweezer-Type
- All makers of Instrument, Manual, Surgical, General Use
- All makers of Accessories, Retractor, Dental
- All makers of Handle, Instrument, Dental
- All makers of Sterilization Wrap Containers, Trays, Cassettes & Other Accessories
- All makers of Plier, Orthodontic
Updated August 2, 2010. 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.