Atlas FDA

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

Techmedica, Inc. — Predicate Candidate Screening

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

90 daysmedian FDA review time
406 days90th percentile
31clearances measured
K-numberDeviceApplicantDecidedReview daysRecalls (K-match)
K933935CKS POROUS COATED FEMORAL COMPONENTTechmedica, Inc.1994-10-114260
K932017TECHMEDICA CONTINUUM HIP WITH HA COATINGTechmedica, Inc.1994-09-014930
K931929TECHMEDICA CONTINUUM HIP SYSTEMTechmedica, Inc.1994-03-293470
K926387TECHMEDICA STANDARD CEMENTED HIP SYSTEMTechmedica, Inc.1994-02-014060
K925420TECHMEDICA STANDARD BIPOLAR SYSTEMTechmedica, Inc.1993-09-283360
K923808MULLER STRAIGHT STEM FEMORAL PROSTHESISTechmedica, Inc.1993-07-273630
K926579TECHMEDICA 6.5MM SELF-TAPPING CANCELLOUS BONE SCRETechmedica, Inc.1993-04-061330
K911058TECHMEDICA CAD/CAM CUSTOM HIPTechmedica, Inc.1993-02-237180
K925181TECHMEDICA MUELLER TYPE POLYETHYLENE ACETBUL CUPTechmedica, Inc.1993-02-051140
K920080CONTINUUM KNEE SYSTEMTechmedica, Inc.1992-09-012370
K921458TMP MICROPLATING SYSTEMTechmedica, Inc.1992-07-171120
K921801MODIFICATION TECHMEDICA MP (MINIPLATING) SYSTEMTechmedica, Inc.1992-07-15930
K921131CKS OSCILLATING SAW BLADETechmedica, Inc.1992-06-08900
K914072CONTINUUM KNEE SYSTEM (CKS)Techmedica, Inc.1992-02-181600
K915187CANCELLOUS BONE-L.P. AND CORTICAL BONE SCREWTechmedica, Inc.1991-12-19310
K905024TMP MANDIBULAR COMPRESSION SYSTEMTechmedica, Inc.1991-06-242290
K903286CONTINUUM KNEE SYSTEM (CKS)-MODIFICATIONTechmedica, Inc.1990-10-12880
K901457CONTINUUM KNEE SYSTEM (CKS)Techmedica, Inc.1990-06-20840
K900619CAAS UNICOMPARMENTAL KNEE SYSTEMTechmedica, Inc.1990-06-111230
K896542ADDITION TO THE CONTINUUM KNEE SYSTEM (CKS(TM))Techmedica, Inc.1990-02-15900
K896369TITANIUM MESH MAXILLOFACIAL IMPLANT SYSTEMTechmedica, Inc.1989-11-24180
K883922TECHMEDICA I.B.O. BLADETechmedica, Inc.1988-12-08830
K882922TECHMEDICA MP SYSTEMTechmedica, Inc.1988-09-22710
K873005TECHMEDICA HEAVYD GAUGE TITANIUM MESH SHEET/STRIPSTechmedica, Inc.1987-09-01280
K841297TECHMEDICA DRILL GUIDETechmedica, Inc.1984-04-25260
K841298HOLE CHAMFERING DEVICETechmedica, Inc.1984-04-25260
K840100PATELLA PROSTHESISTechmedica, Inc.1984-02-09300
K834411TECHMEDICA-HEWSON SHOULDER CLEATTechmedica, Inc.1984-01-17330
K831248PATELLAR FAT PAD RETRACTORTechmedica, Inc.1983-06-24670
K830255OSTEOTOMY BONE STAPLETechmedica, Inc.1983-03-09430
K813567TECHMEDIA BONE STAPLETechmedica, Inc.1982-01-12210

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