510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K844349Substantially Equivalent

Sr Vivodent Pe Anterior Teeth & Sr Orthotyp Re Pos

Ivoclar USA, Inc., Chicago IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K844349 is the FDA 510(k) clearance record for SR VIVODENT PE ANTERIOR TEETH & SR ORTHOTYP RE POS, a class II device, cleared for Ivoclar USA, Inc. on under FDA product code ELM (Denture, Plastic, Teeth). FDA records list 11 510(k) clearances for Ivoclar USA, Inc., from to . As of , FDA records show no recalls naming K844349.

Clearance record

Decision date
Received
(24 days to decision)
Product code
ELM Denture, Plastic, Teeth
Regulation
21 CFR 872.3590
Device class
Class II
Review panel
Dental
Applicant
Ivoclar USA, Inc. Bauer, Cheng & Associates, Chicago IL
Third party review
No

Clearances, product code ELM

Trailing 12 months

FDA records hold no clearances under product code ELM in the trailing twelve months.

FDA records show no clearances under product code ELM in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code ELM, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260