DENTAL BURS— 510(k) K882183

Name: FDA 510(k) clearance K882183
Creator: U.S. Food and Drug Administration
Published: 1988-06-21

Substantially Equivalent

Tri-Stage, Inc.

FDA 510(k) clearance K882183 for DENTAL BURS, Substantially Equivalent on 1988-06-21. Applicant: Tri-Stage, Inc.. Device class: 1.

Clearance details

Applicant: Tri-Stage, Inc.
Product code: Code EJL
Device class: Class 1
Regulation: 21 CFR 872.3240
Advisory panel: Dental
Date received: 1988-05-24
Decision date: 1988-06-21
Decision: Substantially Equivalent
Clearance type: Traditional
Location: San Diego, CA, US

Download summary PDF View on FDA.gov ↗

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K080687 — SMARTBURS2008-06-20
K071352 — CERADRILL2007-06-29
K061383 — BTI STERILE DENTAL DRILLS KIT, BTI ABUTMENTS AND CAPS2006-08-03
K943273 — TRI HAWK BUR, FG BUR1994-08-01
K926205 — MONOSTERYL1994-02-10

More clearances from Tri-Stage, Inc.

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K882834 — TISSUE PUNCH1988-08-02
K880220 — TRI-STAGE (TS-I) DENTAL IMPLANT1988-03-31

Adverse events under product code EJL

product code EJL

Other: 1
Total: 1

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

Data sourced from openFDA. This site is unofficial and independent of the FDA.