ALLOYBOND— 510(k) K981383

Substantially Equivalent

Southern Dental Industries, Inc.

FDA 510(k) clearance K981383 for ALLOYBOND, Substantially Equivalent on 1998-06-16. Applicant: Southern Dental Industries, Inc.. Device class: 2.

Clearance details

Applicant: Southern Dental Industries, Inc.
Product code: Code KLE
Device class: Class 2
Regulation: 21 CFR 872.3200
Advisory panel: Dental
Date received: 1998-04-16
Decision date: 1998-06-16
Decision: Substantially Equivalent
Clearance type: Traditional
Location: San Francisco, CA, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code KLE

K260485 — Any-Etch2026-05-14
K260430 — Porcelain Etch Gel2026-04-10
K252450 — Adhese 22026-03-05
K260682 — Bond-PR Universal Adhesive2026-03-03
K251587 — VITA VMLC Primer2026-02-23

More clearances from Southern Dental Industries, Inc.

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