510(K) CLEARANCES 75 ▼9RECALLS POSTED 26 ▼13CLASS I 2 ▼4PMA DECISIONS 54 ▲7WEEK ENDING / FDA DATA AS OF
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K210203Substantially Equivalent

mmRNA appliance

Vivos Therapeutics, Inc. (Formerly Vivos Biotechnologies, I), Highland Ranch CO / Abbreviated, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K210203 is the FDA 510(k) clearance record for mmRNA appliance, a class II device, cleared for Vivos Therapeutics, Inc. (Formerly Vivos Biotechnologies, I) on under FDA product code LRK (Device, Anti-Snoring). FDA records list one 510(k) clearance for Vivos Therapeutics, Inc. (Formerly Vivos Biotechnologies, I). As of , FDA records show no recalls naming K210203.

Clearance record

Decision date
Received
(205 days to decision)
Product code
LRK Device, Anti-Snoring
Regulation
21 CFR 872.5570
Device class
Class II
Review panel
Dental
Applicant
Vivos Therapeutics, Inc. (Formerly Vivos Biotechnologies, I) 9137 S. Ridgeline Blvd. Suite 135, Highland Ranch CO
510(k) summary
Summary PDF
Third party review
No

Clearances, product code LRK

Trailing 12 months
13 clearances under product code LRK in the twelve months to October 2026, November 2025 the highest month at 3.
Show the numbers
Monthly 510(k) clearances under FDA product code LRK, trailing twelve months
MonthClearances
November 20253
December 20252
January 20260
February 20260
March 20262
April 20261
May 20261
June 20262
July 20261
August 20261
September 20260
October 20260