Cleared Traditional

K030312 - PORTA IMPLANT

K030312 is an FDA 510(k) clearance for PORTA IMPLANT, manufactured by Wieland Dental + Technik GmbH & Co. KG. The device is a Class 2 Dental device with product code EJT cleared through the Traditional 510(k) pathway after a 55-day FDA review.

K030312 · Wieland Dental + Technik GmbH & Co. KG · Dental device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Mar 2003
Decision
55d
Days
Class 2
Risk

K030312 is an FDA 510(k) clearance for the PORTA IMPLANT. Classified as Alloy, Gold-based Noble Metal (product code EJT), Class II - Special Controls.

Submitted by Wieland Dental + Technik GmbH & Co. KG (Pforzheim, DE). The FDA issued a Cleared decision on March 26, 2003 after a review of 55 days - a notably fast clearance cycle.

This device falls under the Dental FDA review panel, regulated under 21 CFR 872.3060 - 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 Wieland Dental + Technik GmbH & Co. KG devices

FDA 510(k) Submission Details - K030312

510(k) Number K030312 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received January 30, 2003
Decision Date March 26, 2003
Days to Decision 55 days
Submission Type Traditional
Review Panel Dental (DE)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
72d faster than avg
Panel avg: 127d · This submission: 55d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

EJT Device Classification - Class 2, Special Controls

Product Code EJT Alloy, Gold-based Noble Metal
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 872.3060
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 - EJT Alloy, Gold-based Noble Metal

All 549
Devices cleared under the same product code (EJT) and FDA review panel - the closest regulatory comparables to K030312.
PORTA PRESSOVER
K031264 · Wieland Dental + Technik GmbH & Co. KG · Jun 2003
BIOUNIVERSAL PKF
K030435 · Ivoclar Vivadent, Inc. · Apr 2003
BIO UNIVERSAL
K030436 · Ivoclar Vivadent, Inc. · Apr 2003
PORTADUR P2
K023395 · Wieland Dental + Technik GmbH & Co. KG · Dec 2002
BIOPORTA G
K023391 · Wieland Dental + Technik GmbH & Co. KG · Dec 2002
PORTA GEO TI
K023389 · Wieland Dental + Technik GmbH & Co. KG · Dec 2002