ERCH ARCH BAR, MODEL 38-690-00— 510(k) K061271

Substantially Equivalent

KLS-Martin L.P.

FDA 510(k) clearance K061271 for ERCH ARCH BAR, MODEL 38-690-00, Substantially Equivalent on 2006-06-30. Applicant: KLS-Martin L.P.. Device class: 2.

Clearance details

Applicant: KLS-Martin L.P.
Product code: Code DYX
Device class: Class 2
Regulation: 21 CFR 872.4600
Advisory panel: Dental
Date received: 2006-05-05
Decision date: 2006-06-30
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Jacksonville, FL, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code DYX

K162046 — MINNE TIES MMF Suture System2017-04-11
K031207 — SAFETY RELEASE ARCH BAR KIT2003-07-15
K030605 — RAPID IMF2003-06-27
K990212 — LOCKJAW 15 MINUTE INTERMAXILLARY FIXATION SYSTEM,MODEL LJ100-001999-09-14
K991004 — SYNTHES QUICK LOCK IMF SYSTEM1999-06-23

More clearances from KLS-Martin L.P.

K260137 — KLS Martin IPS Oral-Max Implants - MR Conditional +3 more2026-08-17
K253660 — KLS Martin Pure Pectus System2026-02-20
K254162 — KLS Martin Ixos System2026-02-20
K250988 — KLS Martin Pure Pectus System2025-12-11
K250865 — KLS Martin IPS Forearm System2025-11-14

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