510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K935082Substantially Equivalent

3M Dental Electronic Anesthesia (Dea) System 8670 Modification

3M Company, St. Paul MN / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K935082 is the FDA 510(k) clearance record for 3M DENTAL ELECTRONIC ANESTHESIA (DEA) SYSTEM 8670 MODIFICATION, cleared for 3M Company on under FDA product code LWM (Device, Electrical Dental Anesthesia). FDA records list 146 510(k) clearances for 3M Company, from to . As of , FDA records show no recalls naming K935082.

Clearance record

Decision date
Received
(96 days to decision)
Product code
LWM Device, Electrical Dental Anesthesia
Device class
Unclassified
Review panel
Unknown
Applicant
3M Company 3m Center, St. Paul MN
510(k) summary
Summary
Third party review
No

Clearances, product code LWM

Trailing 12 months

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

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