510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K120338Substantially Equivalent

Atlantis in Zirconia for Dentsply Ankylos Implant, Atlantis Later Abutment in Zirconia

Astra Tech, Inc., Skokie IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K120338 is the FDA 510(k) clearance record for ATLANTIS IN ZIRCONIA FOR DENTSPLY ANKYLOS IMPLANT, ATLANTIS LATER ABUTMENT IN ZIRCONIA, a class II device, cleared for Astra Tech, 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 38 510(k) clearances for Astra Tech, Inc., from to . As of , FDA records show no recalls naming K120338.

Clearance record

Decision date
Received
(153 days to decision)
Product code
NHA Abutment, Implant, Dental, Endosseous
Regulation
21 CFR 872.3630
Device class
Class II
Review panel
Dental
Applicant
Astra Tech, Inc. 8944 Tamaroa Ter., Skokie IL
510(k) summary
Summary PDF
Third party review
No

Clearances, product code NHA

Trailing 12 months
29 clearances under product code NHA in the twelve months to October 2026, June 2026 the highest month at 6.
Show the numbers
Monthly 510(k) clearances under FDA product code NHA, trailing twelve months
MonthClearances
November 20253
December 20254
January 20265
February 20261
March 20261
April 20262
May 20263
June 20266
July 20261
August 20261
September 20262
October 20260