510(K) CLEARANCES 49 ▼18RECALLS POSTED 23 ▼3CLASS I 1 ▼1PMA DECISIONS 37 ▼3WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
SUBSCRIBE / SIGN IN
K121688Substantially Equivalent

Multi-Unit Abutments with Angulations 17 and 30 for Tapered Implant System

Prismatik Dentalcraft, Inc., Irvine CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K121688 is the FDA 510(k) clearance record for MULTI-UNIT ABUTMENTS WITH ANGULATIONS 17 AND 30 FOR TAPERED IMPLANT SYSTEM, a class II device, cleared for Prismatik Dentalcraft, Inc. on under FDA product code NHA (Abutment, Implant, Dental, Endosseous). FDA's definition for product code NHA reads: "To be used in conjunction with an endosseous dental implant fixture to aid in prosthetic rehabilitation". FDA records list 58 510(k) clearances for Prismatik Dentalcraft, Inc., from to . As of , FDA records show no recalls naming K121688.

Clearance record

Decision date
Received
(127 days to decision)
Product code
NHA Abutment, Implant, Dental, Endosseous
Regulation
21 CFR 872.3630
Device class
Class II
Review panel
Dental
Applicant
Prismatik Dentalcraft, Inc. 2212 Dupont Dr., St. P, Irvine CA
510(k) summary
Summary PDF
Third party review
No

Clearances, product code NHA

Trailing 12 months
27 clearances under product code NHA in the twelve months to November 2026, June 2026 the highest month at 6.
Show the numbers
Monthly 510(k) clearances under FDA product code NHA, trailing twelve months
MonthClearances
December 20254
January 20265
February 20261
March 20261
April 20262
May 20263
June 20266
July 20261
August 20261
September 20263
October 20260
November 20260