510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K100360Substantially Equivalent

Bia300 Series Implant and Abutment, Bi300 Implant, Ba300 Abutment

Cochlear Americas, Centennial CO / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K100360 is the FDA 510(k) clearance record for BIA300 SERIES IMPLANT AND ABUTMENT, BI300 IMPLANT, BA300 ABUTMENT, a class II device, cleared for Cochlear Americas on under FDA product code LXB (Hearing Aid, Bone Conduction). FDA records list 21 510(k) clearances for Cochlear Americas, from to . As of , FDA records show no recalls naming K100360.

Clearance record

Decision date
Received
(151 days to decision)
Product code
LXB Hearing Aid, Bone Conduction
Regulation
21 CFR 874.3302
Device class
Class II
Review panel
Ear, Nose, Throat
Applicant
Cochlear Americas 13059 E Peakview Ave., Centennial CO
510(k) summary
Statement
Third party review
No

Clearances, product code LXB

Trailing 12 months
4 clearances under product code LXB in the twelve months to October 2026, June 2026 the highest month at 2.
Show the numbers
Monthly 510(k) clearances under FDA product code LXB, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20262
July 20261
August 20261
September 20260
October 20260