J. MORITA FLEX M-3 TORX HARDPIECE— 510(k) K821739

Name: FDA 510(k) clearance K821739
Creator: U.S. Food and Drug Administration
Published: 1982-06-25

Substantially Equivalent

Pacific Dental Corp.

FDA 510(k) clearance K821739 for J. MORITA FLEX M-3 TORX HARDPIECE, Substantially Equivalent on 1982-06-25. Applicant: Pacific Dental Corp.. Device class: 1.

Clearance details

Applicant: Pacific Dental Corp.
Product code: Code EKX
Device class: Class 1
Regulation: 21 CFR 872.4200
Advisory panel: Dental
Date received: 1982-06-14
Decision date: 1982-06-25
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code EKX

view all

K261987 — Reusable SmartPeg2026-09-08
K252223 — Alpha Endo Handpiece (Alpha Endo)2025-10-16
K251597 — InnerView System2025-09-18
K243692 — EnDrive (EnDriveUS)2025-08-22
K242514 — Endo Motor (E-LITE MAX, E-LITE PRO, E-LITE INO)2025-04-24

More clearances from Pacific Dental Corp.

view all

K821782 — BEACH ANESTHETIC SYRINGE CARTR. TYPE1982-07-20
K821777 — BEACH MOUTH MIRROR1982-07-06
K821778 — BEACH DRESSING PLIER1982-07-06
K821779 — BEACH AMALGAM CARRIER, GUN TYPE1982-07-06
K821780 — BEACH EXPLORER NO. 23T.G.1982-07-06

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