Data / Medical devices / Canada / E/T Endodontic Technologies, Ltd.
E/T Endodontic Technologies, Ltd.: FDA-registered device maker in HALIFAX Nova Scotia, Canada, 3 510(k) clearances
E/T Endodontic Technologies, Ltd. is registered with the FDA (registration 3004569445) in HALIFAX Nova Scotia, Canada. It lists 14 device types. The FDA files 3 510(k) clearances under its listings, the newest dated April 20, 2005. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3004569445
- Address
- 389 - 5991 Spring Garden RD., HALIFAX Nova Scotia, Canada, B3H 1Y6
- Owner or operator
- E/T ENDODONTIC TECHNOLOGIES, LTD. (9063656)
- Roles
- Exporter to the US, Repackager or relabeler
- First device listed
- May 20, 2004
- Registered through
- 2026
- Brand names listed
- AH PLUS SEALER, ANTAEOS BARBED BROACHES, Acteon IrriSafe Tips, CHELATE, ISOLATE PREMIUM DENTAL DAM, KERR EWT SEALER, MANI Dia-Burs, MANI Finger Pluggers and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Broach, Endodontic | EKW | 1 | Exporter to the US | accessdata.fda.gov |
| Bur, Dental | EJL | 1 | Exporter to the US | accessdata.fda.gov |
| Cement, Dental | EMA | 2 | Exporter to the US, Repackager or relabeler | accessdata.fda.gov |
| Dam, Rubber | EIE | 1 | Exporter to the US, Repackager or relabeler | accessdata.fda.gov |
| Drill, Dental, Intraoral | DZA | 1 | Exporter to the US | accessdata.fda.gov |
| File, Pulp Canal, Endodontic | EKS | 1 | Exporter to the US | accessdata.fda.gov |
| Instrument, Diamond, Dental | DZP | 1 | Exporter to the US | accessdata.fda.gov |
| Liner, Cavity, Calcium Hydroxide | EJK | 2 | Exporter to the US | accessdata.fda.gov |
| Mirror, Mouth | EAX | 1 | Exporter to the US | accessdata.fda.gov |
| Plugger, Root Canal, Endodontic | EKR | 1 | Exporter to the US | accessdata.fda.gov |
| Preparer, Root Canal Endodontic | EKQ | 1 | Exporter to the US | accessdata.fda.gov |
| Reamer, Pulp Canal, Endodontic | EKP | 1 | Exporter to the US | accessdata.fda.gov |
| Scaler, Ultrasonic | ELC | 2 | Exporter to the US | accessdata.fda.gov |
| Spreader, Pulp Canal Filling Material, Endodontic | EKK | 1 | Exporter to the US | 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 |
|---|---|---|---|---|---|---|
| April 20, 2005 | K050895 | SURPASSON P5 NEWTRON | ELC | Substantially Equivalent | Satelec | accessdata.fda.gov |
| January 5, 1998 | K974140 | ADHESIVE HYBRID IONOMER CEMENT | EMA | Substantially Equivalent | Dentsply Intl. | accessdata.fda.gov |
| November 30, 1994 | K944945 | PULPDENT CALCIUM HYDROXIDE PREPARATIONS | EJK | Substantially Equivalent | Pulpdent Corp. | accessdata.fda.gov |
Compare with other makers
- All makers of Spreader, Pulp Canal Filling Material, Endodontic
- All makers of Scaler, Ultrasonic
- All makers of Instrument, Diamond, Dental
- All makers of Cement, Dental
- All makers of Reamer, Pulp Canal, Endodontic
- All makers of Bur, Dental
Updated April 20, 2005. 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.