Atlas FDA

LYTHOS DIGITAL IMPRESSION SYSTEM

FDA 510(k) clearance K141611 · decided 2014-12-05

Clearance details

K-number
K141611
Device name
LYTHOS DIGITAL IMPRESSION SYSTEM
Applicant
Ormco Corp.
Decision
Substantially Equivalent
Date received
2014-06-16
Decision date
2014-12-05
Days to decision
172 days
Clearance type
Traditional
Product code
NOF
Device class
2
Regulation number
872.3661
Medical specialty
Dental
Advisory committee
Dental
Location
Orange, CA, US
Third-party review
No
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
DIGITAL IMPRESSION SYSTEM FOR ORTHODONTIC USE (K122065)Ormco Corp.2013-02-08
3M TRUE DEFINITION SCANNER (K122467)3M Company2012-11-20
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.