510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K823209Substantially Equivalent

Bioself 101

Bioself, Inc., Mchenry IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K823209 is the FDA 510(k) clearance record for BIOSELF 101, cleared for Bioself, Inc. on under FDA product code LHD (Device, Fertility Diagnostic, Proceptive). FDA records list 3 510(k) clearances for Bioself, Inc., from to . As of , FDA records show no recalls naming K823209.

Clearance record

Decision date
Received
(110 days to decision)
Product code
LHD Device, Fertility Diagnostic, Proceptive
Device class
Unclassified
Review panel
Unknown
Applicant
Bioself, Inc. 803 N. Front St. Suite 3, Mchenry IL
Third party review
No

Clearances, product code LHD

Trailing 12 months

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

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