510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K770636Substantially Equivalent

Table, Exam & Manupulation

I E Industries, Mchenry IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K770636 is the FDA 510(k) clearance record for TABLE, EXAM & MANUPULATION, a class I device, cleared for I E Industries on under FDA product code INT (Plinth). FDA records list 3 510(k) clearances for I E Industries, from to . As of , FDA records show no recalls naming K770636.

Clearance record

Decision date
Received
(11 days to decision)
Product code
INT Plinth
Regulation
21 CFR 890.3520
Device class
Class I
Review panel
Physical Medicine
Applicant
I E Industries 803 N. Front St. Suite 3, Mchenry IL
Third party review
No

Clearances, product code INT

Trailing 12 months

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

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