Atlas FDA

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

Mis Implants Technologies , Ltd. — Predicate Candidate Screening

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

142 daysmedian FDA review time
353 days90th percentile
13clearances measured
K-numberDeviceApplicantDecidedReview daysRecalls (K-match)
K182228MIS LOCKiT Abutments System, OT-Equators and Ball AttachmentMis Implants Technologies , Ltd.2019-01-281650
K180282MIS Internal Hex Dental Implant SystemMis Implants Technologies , Ltd.2018-06-221420
K173326MIS CONNECT Conical Connection AbutmentMis Implants Technologies , Ltd.2018-03-161470
K172505MIS C1 Narrow Platform Conical Connection Implant System, MIMis Implants Technologies , Ltd.2017-12-281320
K163349MIS V3 Conical Connection Dental Implant System­Mis Implants Technologies , Ltd.2017-05-261780
K112162CONICAL CONNECTION IMPLANTSMis Implants Technologies , Ltd.2012-08-083780
K110750PERIOPATCHMis Implants Technologies , Ltd.2011-04-28420
K101014BOND BONEMis Implants Technologies , Ltd.2010-10-211920
K092555UNO NARROW IMPLANTMis Implants Technologies , Ltd.2010-01-051380
K080162UNO - ONE PIECE SCREW-TYPE DENTAL IMPLANTMis Implants Technologies , Ltd.2008-04-22900
K073461ORTHO ANCHOR SCREWSMis Implants Technologies , Ltd.2008-01-25460
K070022MISTRAL - ONE STAGE SCREW-TYPE DENTAL IMPLANT, MODEL MF9Mis Implants Technologies , Ltd.2007-04-201070
K003191MIS IMPLANT SYSTEM DECIVEMis Implants Technologies , Ltd.2001-09-283530

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