510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K830849Substantially Equivalent

Ob Tilt

Lic-Orthion, Mchenry IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K830849 is the FDA 510(k) clearance record for OB TILT, a class I device, cleared for Lic-Orthion on under FDA product code INQ (Table, Powered). FDA records list 17 510(k) clearances for Lic-Orthion, from to . As of , FDA records show no recalls naming K830849.

Clearance record

Decision date
Received
(19 days to decision)
Product code
INQ Table, Powered
Regulation
21 CFR 890.3760
Device class
Class I
Review panel
Physical Medicine
Applicant
Lic-Orthion 803 N. Front St. Suite 3, Mchenry IL
Third party review
No

Clearances, product code INQ

Trailing 12 months

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

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