510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
SUBSCRIBE / SIGN IN
K920069Substantially Equivalent

Magni-Cam

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

K920069 is the FDA 510(k) clearance record for MAGNI-CAM, a class I device, cleared for Innoventions, Inc. on under FDA product code HJG (System, Reading, Television, Closed-Circuit). FDA records list one 510(k) clearance for Innoventions, Inc. As of , FDA records show no recalls naming K920069.

Clearance record

Decision date
Received
(55 days to decision)
Product code
HJG System, Reading, Television, Closed-Circuit
Regulation
21 CFR 886.5820
Device class
Class I
Review panel
Ophthalmic
Applicant
Innoventions, Inc. 12 Robin Crest Ln., Ltttleton CO
510(k) summary
Summary
Third party review
No

Clearances, product code HJG

Trailing 12 months

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

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