Atlas FDA

3M TRUE DEFINITION SCANNER

FDA 510(k) clearance K122467 · decided 2012-11-20

Clearance details

K-number
K122467
Device name
3M TRUE DEFINITION SCANNER
Applicant
3M Company
Decision
Substantially Equivalent
Date received
2012-08-13
Decision date
2012-11-20
Days to decision
99 days
Clearance type
Traditional
Product code
NOF
Device class
2
Regulation number
872.3661
Medical specialty
Dental
Advisory committee
Dental
Location
Saint Paul, MN, US
Third-party review
Yes
Expedited review
No

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Similar devices under this product code

Devices cleared under the same product code - the starting set for predicate research.

RecordFirmDate
LYTHOS DIGITAL IMPRESSION SYSTEM (K141611)Ormco Corp.2014-12-05
DIGITAL IMPRESSION SYSTEM FOR ORTHODONTIC USE (K122065)Ormco Corp.2013-02-08
3M UNITEK LAVA CHAIRSIDE ORAL SCANNER (K081961)Brontes Technologies2008-09-05
3M ESPE LAVA CHAIRSIDE ORAL SCANNER (K073199)Brontes Technologies2007-12-21

Recalls involving this device

No recalls on record reference this clearance.

PMA approvals by this applicant

RecordFirmDate
KENNEDY LAD(TM) LIGAMENT AUGMENTATION DEVICE (P850069/S011)3M Company1994-11-28
CENNEDY LAD(TM) LIGAMENT AUGMENTATION DEVICE (P850069/S010)3M Company1994-05-19
KENNEDY LAD(TM) LIGAMENT AUGMENTATION DEVICE (P850069/S006)3M Company1992-12-31
KENNEDY LAD(TM) LIGAMENT AUGMENTATION DEVICE (P850069/S009)3M Company1992-03-13
KENNEDY LAD(TM) LIGAMENT AUGMENTATION DEVICE (P850069/S008)3M Company1992-01-28
KENNEDY LAD(TM) LIGAMENT AUGMENTATION DEVICE (P850069/S007)3M Company1990-10-17
KENNEDY LAD(TM) LIGAMENT AUGMENTATION DEVICE (P850069/S005)3M Company1990-03-08
KENNEDY LAD(TM) LIGAMENT AUGMENTATION DEVICE (P850069/S004)3M Company1989-11-22