510(K) CLEARANCES 67 ▼8RECALLS POSTED 26CLASS I 2PMA DECISIONS 40 ▼14WEEK ENDING / FDA DATA AS OF
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K902050Substantially Equivalent

Biolastic Super Elastic Arches

Rmo, Inc., Denver CO / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K902050 is the FDA 510(k) clearance record for BIOLASTIC SUPER ELASTIC ARCHES, a class I device, cleared for Rmo, Inc. on under FDA product code EJF (Bracket, Metal, Orthodontic). FDA records list one 510(k) clearance for Rmo, Inc. As of , FDA records show no recalls naming K902050.

Clearance record

Decision date
Received
(88 days to decision)
Product code
EJF Bracket, Metal, Orthodontic
Regulation
21 CFR 872.5410
Device class
Class I
Review panel
Dental
Applicant
Rmo, Inc. Post Office Box 17085, Denver CO
Third party review
No

Clearances, product code EJF

Trailing 12 months

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

FDA records show no clearances under product code EJF in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code EJF, 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