510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K823149Substantially Equivalent

Ob Tilt Table

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

K823149 is the FDA 510(k) clearance record for OB TILT TABLE, a class I device, cleared for Orthion Corp. on under FDA product code INW (Table, Mechanical). FDA records list 11 510(k) clearances for Orthion Corp., from to . As of , FDA records show no recalls naming K823149.

Clearance record

Decision date
Received
(16 days to decision)
Product code
INW Table, Mechanical
Regulation
21 CFR 890.3750
Device class
Class I
Review panel
Physical Medicine
Applicant
Orthion Corp. 803 N. Front St. Suite 3, Mchenry IL
Third party review
No

Clearances, product code INW

Trailing 12 months

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

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