ClearanceBrief
Company ยท US

Midwest

FDA 510(k) clearances and medical device recalls filed under this name, 1976 to 1986. Name variants (Inc, Corp, punctuation) are merged.

13510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
EAYLight, Fiber Optic, Dental5
EFBHandpiece, Air-Powered, Dental5
EGSHandpiece, Contra- And Right-Angle Attachment, Dental2
EBFMaterial, Tooth Shade, Resin1

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Oct 6, 1986K863677TRADITION HIGH SPEED HANDPIECE
Midwest
EFB
Mar 25, 1985K850344AM-40 POWER OPTIC AIR MOTOR POWER OPTIC CONTRA ANG
Midwest
EGS
Dec 6, 1979K792445MW STRAIGHT ATTACHMENT
Midwest
EGS
Nov 27, 1979K792304MW-8000
Midwest
EFB
Nov 27, 1979K792303MW 8000-I
Midwest
EBF
Nov 27, 1979K792302LS-100
Midwest
EFB
Nov 20, 1979K791771ORALUMINATOR III AUTO-LIGHT
Midwest
EAY
Oct 23, 1979K791733LIGHT-PAK
Midwest
EAY
Feb 26, 1979K790113MIDWEST 1000
Midwest
EFB
Dec 29, 1978K781878LIGHT, INSIDE
Midwest
EAY
Oct 20, 1976K760796ORALUMINATOR III - LIGHT SOURCE FOR F.O.
Midwest
EAY
Oct 20, 1976K760795FIBER OPTICS DENTAL HOSE W/INTEGRAL L.C.
Midwest
EAY
Oct 20, 1976K760794FIBER OPTICS HIGH SPEED HANDPIECE
Midwest
EFB

Latest recalls

DateFirm and productCodeLinked 510(k)
No recalls in this window.
Get alerts for these product codes