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
LXVUnclassified

Apparatus, Vestibular Analysis

Unknown
FDA source (opens on fda.gov)

LXV is the FDA product code for Apparatus, Vestibular Analysis. As of , FDA records hold 22 510(k) clearances under this code, the most recent dated , and 2 recalls.

Classification record

Product code
LXV
Device name
Apparatus, Vestibular Analysis
Device class
Unclassified
Review panel
Unknown
Submission type
510(k)
Implant
No
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
No
Ingested clearances
22
Ingested recalls
2

Clearances, product code LXV

By decision year
22 clearances under product code LXV with a decision year between 1977 and 2022, 1989 the highest year at 2.
Show the numbers
510(k) clearances under FDA product code LXV by decision year
YearClearances
19771
19781
19851
19871
19892
19911
19921
19981
20072
20082
20091
20101
20121
20181
20192
20202
20221

Applicants with the most clearances

Product code LXV
Applicants holding the most 510(k) clearances under product code LXV
ApplicantClearances
Interacoustics a/S3
Micromedical Technologies, Inc.2
Breg, Inc.1
Capacity Sports, LLC1
Chattanooga Group, Inc.1
Clearwater Clinical Limited1
Contraves1
Contraves Goerz Corp.1
Ics Medical Corp.1
King-Devick Technologies, Inc1

Companies listing this code with FDA

Companies whose registered establishments list this code