Data / Medical devices / United States / Medequip Implant Supplies
Medequip Implant Supplies: FDA-registered device maker in Jupiter, FL, United States, 1 510(k) clearance
Medequip Implant Supplies is registered with the FDA (registration 3011103459) in Jupiter, FL, United States. It lists 3 device types. The FDA files 1 510(k) clearance under its listings, the newest dated March 20, 1996. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3011103459
- Address
- 612 N Orange Ave Ste D10, Jupiter, FL, United States, 33458
- Owner or operator
- Medequip Implant Supplies (10047373)
- Roles
- Repackager or relabeler
- First device listed
- August 18, 2014
- Registered through
- 2026
- Brand names listed
- Dental Hand Instrument, Dental implants, guidance system
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Accessories, Implant, Dental, Endosseous | NDP | 1 | Repackager or relabeler | accessdata.fda.gov |
| Curette, Surgical, Dental | EMK | 1 | Repackager or relabeler | accessdata.fda.gov |
| Implant, Endosseous, Root-Form | DZE | 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 20, 1996 | K960110 | KIS MT3 | DZE | Substantially Equivalent | The Implant Center of the Palm Beaches | accessdata.fda.gov |
Compare with other makers
- All makers of Accessories, Implant, Dental, Endosseous
- All makers of Implant, Endosseous, Root-Form
- All makers of Curette, Surgical, Dental
Updated March 20, 1996. 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.