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
K111342Substantially Equivalent

Light Guide Cable

Schott North America, North Attleboro MA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K111342 is the FDA 510(k) clearance record for LIGHT GUIDE CABLE, a class II device, cleared for Schott North America on under FDA product code HBI (Illuminator, Fiberoptic, Surgical Field). FDA records list one 510(k) clearance for Schott North America. As of , FDA records show no recalls naming K111342.

Clearance record

Decision date
Received
(196 days to decision)
Product code
HBI Illuminator, Fiberoptic, Surgical Field
Regulation
21 CFR 878.4580
Device class
Class II
Review panel
General, Plastic Surgery
Applicant
Schott North America 40 Plain St., North Attleboro MA
510(k) summary
Summary PDF
Third party review
No

Clearances, product code HBI

Trailing 12 months

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

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