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

Device, Electrical Dental Anesthesia

Unknown
FDA source (opens on fda.gov)

LWM is the FDA product code for Device, Electrical Dental Anesthesia. As of , FDA records hold 15 510(k) clearances under this code, the most recent dated , and no recalls.

Classification record

Product code
LWM
Device name
Device, Electrical Dental Anesthesia
Device class
Unclassified
Review panel
Unknown
Submission type
510(k)
Implant
No
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
No
Ingested clearances
15
Ingested recalls
0

Clearances, product code LWM

By decision year
15 clearances under product code LWM with a decision year between 1987 and 2020, 1992 the highest year at 3.
Show the numbers
510(k) clearances under FDA product code LWM by decision year
YearClearances
19871
19881
19891
19902
19923
19943
20011
20191
20202

Applicants with the most clearances

Product code LWM
Applicants holding the most 510(k) clearances under product code LWM
ApplicantClearances
Synapse Dental3
3M Company2
M. D. Products2
3M Company1
3M Company1
D-W Intl.1
Electronic Waveform Laboratory, Inc.1
Medical Consultants Intl., Ltd.1
Pain Prevention Laboratory, Inc.1
Satelec1

Companies listing this code with FDA

Companies whose registered establishments list this code