510(K) CLEARANCES 67 ▼8RECALLS POSTED 26CLASS I 2PMA DECISIONS 40 ▼14WEEK ENDING / FDA DATA AS OF
Medical Device
Manufacturing
THE TRADE PAPER OF THE FACTORY FLOOR
K051812Substantially Equivalent

Tgo Spray

Laboratoires Carilene S.A.S., Washington DC / Traditional, Substantially Equivalent

K051812 is the FDA 510(k) clearance record for TGO SPRAY, cleared for Laboratoires Carilene S.A.S. on under FDA product code LFD (Saliva, Artificial). FDA records list one 510(k) clearance for Laboratoires Carilene S.A.S. As of , FDA records show no recalls naming K051812.

Clearance record

Decision date
Received
(108 days to decision)
Product code
LFD Saliva, Artificial
Device class
Unclassified
Review panel
Unknown
Applicant
Laboratoires Carilene S.A.S. 1800 Massachusetts Ave. NW, Washington DC
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