Atlas FDA

Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account

Technolas Perfect Vision GmbH — Predicate Candidate Screening

10 FDA 510(k) clearances under this manufacturer; the 50 most recent screened below.

185 daysmedian FDA review time
281 days90th percentile
10clearances measured
K-numberDeviceApplicantDecidedReview daysRecalls (K-match)
K200724VICTUS Femtosecond Laser PlatformTechnolas Perfect Vision GmbH2020-09-011660
K171014VICTUS Femtosecond Laser PlatformTechnolas Perfect Vision GmbH2017-10-191980
K151161VICTUS Femtosecond Laser PlatformTechnolas Perfect Vision GmbH2015-06-24540
K141379VICTUS FEMTOSECOND LASER PLATFORMTechnolas Perfect Vision GmbH2015-01-162340
K140615VICTUS FEMTOSECOND LASER PLATFORMTechnolas Perfect Vision GmbH2014-07-151270
K132534VICTUS FEMTOSECOND LASER PLATFORMTechnolas Perfect Vision GmbH2014-02-141850
K122386VICTUS FEMTOSECOND LASER PLATFORMTechnolas Perfect Vision GmbH2013-02-081860
K120426VICTUS LASER PLATFORMTechnolas Perfect Vision GmbH2012-07-311690
K110427FEMTEC LASER SYSTEM FOR CAPSULOTOMYTechnolas Perfect Vision GmbH2011-11-222810
K984443ORBSCANTechnolas Perfect Vision GmbH1999-03-05810

Methodology

Recall counts reflect FDA recall records explicitly referencing each K-number; FDA links recalls to K-numbers inconsistently, so 0 means "none found in FDA records," not "never recalled." Data: FDA openFDA, refreshed weekly. Verify decisions of consequence against the primary source. Full candidate set and CSV export: atlasbyauro.com.

Prepared with Atlas

Predicate research, review-time statistics and recall monitoring for 510(k) teams — atlasbyauro.com/fda