510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K190144Substantially Equivalent

MucoPEG

Sunbio,Inc., Gunpo-Si, KR / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K190144 is the FDA 510(k) clearance record for MucoPEG, cleared for Sunbio, Inc. on under FDA product code LFD (Saliva, Artificial). FDA records list one 510(k) clearance for Sunbio, Inc. As of , FDA records show no recalls naming K190144.

Clearance record

Decision date
Received
(280 days to decision)
Product code
LFD Saliva, Artificial
Device class
Unclassified
Review panel
Unknown
Applicant
Sunbio, Inc. 95 Sanbon-Ro, Gunpo-Si, KR
510(k) summary
Summary PDF
Third party review
No

Clearances, product code LFD

Trailing 12 months
1 clearance under product code LFD in the twelve months to October 2026, February 2026 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code LFD, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20261
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260