Cleared Traditional

K961754 - SAFETY RELEASE MODULE

K961754 is an FDA 510(k) clearance for SAFETY RELEASE MODULE, manufactured by G & H Wire Co.. The device is a Class 2 Dental device with product code DZB cleared through the Traditional 510(k) pathway after a 65-day FDA review.

K961754 · G & H Wire Co. · Dental device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Jul 1996
Decision
65d
Days
Class 2
Risk

K961754 is an FDA 510(k) clearance for the SAFETY RELEASE MODULE. Classified as Headgear, Extraoral, Orthodontic (product code DZB), Class II - Special Controls.

Submitted by G & H Wire Co. (Greenwood, US). The FDA issued a Cleared decision on July 10, 1996 after a review of 65 days - a notably fast clearance cycle.

This device falls under the Dental FDA review panel, regulated under 21 CFR 872.5500 - the FDA dental device regulatory framework. The Traditional 510(k) pathway establishes clearance through substantial equivalence to a legally marketed predicate device, without requiring clinical trial data.

Device pattern: Fast-track predicate clearance. Standard predicate reliance. The short review cycle indicates strong predicate alignment - the FDA found sufficient equivalence without extended technical review.

View all G & H Wire Co. devices

FDA 510(k) Submission Details - K961754

510(k) Number K961754 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received May 06, 1996
Decision Date July 10, 1996
Days to Decision 65 days
Submission Type Traditional
Review Panel Dental (DE)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
62d faster than avg
Panel avg: 127d · This submission: 65d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

DZB Device Classification - Class 2, Special Controls

Product Code DZB Headgear, Extraoral, Orthodontic
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 872.5500
What this classification means

Class II devices require demonstration of substantial equivalence to a legally marketed predicate device. This pathway does not require clinical trials - it relies on engineering equivalence and performance data. Most Dental devices follow this clearance model.

Regulatory Peers - DZB Headgear, Extraoral, Orthodontic

All 11
Devices cleared under the same product code (DZB) and FDA review panel - the closest regulatory comparables to K961754.
NITOM LOCKING FACEBOW
K980245 · Ortho Kinetics Corp. · Apr 1998
RELEASABLE FORCE MODULE
K980151 · Ortho Kinetics Corp. · Apr 1998
FACEBOW
K980195 · Ortho Kinetics Corp. · Mar 1998
EXTRAORAL HEADGEAR
K936151 · Dentauraum, Inc. · Aug 1994
ADP FACEMASK
K923556 · Ormco Corp. · Dec 1992
HOOD GEAR (TM) BREAKAWAY HEADGEAR W/ HIGH PULL
K902645 · Ormco Corp. · Sep 1990