Data / Medical devices / United States / Basic Dental Implant Systems, Inc.
Basic Dental Implant Systems, Inc.: FDA-registered device maker in Rio Rancho, NM, United States, 3 510(k) clearances
Basic Dental Implant Systems, Inc. is registered with the FDA (registration 1723412) in Rio Rancho, NM, United States. It lists 7 device types. The FDA files 3 510(k) clearances under its listings, the newest dated December 4, 2008. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 1723412
- FEI number
- 3000203940
- Address
- 103 NM HIGHWAY 528 NE Ste B3, Rio Rancho, NM, United States, 87124
- Owner or operator
- Basic Dental Implant Systems, Inc. (9021906)
- Roles
- Manufacturer, Repackager or relabeler
- First device listed
- October 7, 1998
- Registered through
- 2026
- Brand names listed
- Abutment Driver, Abutment Driver Multi-unit, Basic Dental Implant System, DRILL EXTENDER, Depth Gauge-Short&Long, Double End Implant Driver, EMERGENCE PROFILER, HAND BONE DRILL and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Accessories, Implant, Dental, Endosseous | NDP | 1 | Manufacturer | accessdata.fda.gov |
| Bur, Dental | EJL | 1 | Manufacturer | accessdata.fda.gov |
| Crown, Preformed | ELZ | 1 | Manufacturer | accessdata.fda.gov |
| Gauge, Depth, Instrument, Dental | EIL | 1 | Manufacturer | accessdata.fda.gov |
| Handle, Instrument, Dental | EJB | 1 | Manufacturer | accessdata.fda.gov |
| Implant, Endosseous, Root-Form | DZE | 2 | Manufacturer | accessdata.fda.gov |
| Punch, Biopsy, Surgical | EME | 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 |
|---|---|---|---|---|---|---|
| December 4, 2008 | K082749 | OMNI-TIGHT | DZE | Substantially Equivalent | Basic Dental Implant Systems, Inc. | accessdata.fda.gov |
| May 9, 2008 | K072595 | OMNI-TIGHT | DZE | Substantially Equivalent | Basic Dental Implant Systems, Inc. | accessdata.fda.gov |
| November 28, 2001 | K013682 | MODIFICATION TO BASIC DENTAL IMPLANT SYSTEM | DZE | Substantially Equivalent | Basic Dental Implant Systems, Inc. | accessdata.fda.gov |
Compare with other makers
- All makers of Crown, Preformed
- All makers of Bur, Dental
- All makers of Gauge, Depth, Instrument, Dental
- All makers of Implant, Endosseous, Root-Form
- All makers of Handle, Instrument, Dental
- All makers of Punch, Biopsy, Surgical
Updated December 4, 2008. 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.