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
K030829Substantially Equivalent

Vpt Meter

Xilas Medical, Inc., San Antonio TX / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K030829 is the FDA 510(k) clearance record for VPT METER, a class I device, cleared for Xilas Medical, Inc. on under FDA product code LLN (Device, Vibration Threshold Measurement). FDA records list 2 510(k) clearances for Xilas Medical, Inc., from to . As of , FDA records show no recalls naming K030829.

Clearance record

Decision date
Received
(266 days to decision)
Product code
LLN Device, Vibration Threshold Measurement
Regulation
21 CFR 882.1200
Device class
Class I
Review panel
Neurology
Applicant
Xilas Medical, Inc. 12665 Silicon Dr., San Antonio TX
510(k) summary
Summary PDF
Third party review
No

Clearances, product code LLN

Trailing 12 months

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

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