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

Implant Technology, Inc. — Predicate Candidate Screening

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

64 daysmedian FDA review time
177 days90th percentile
13clearances measured
K-numberDeviceApplicantDecidedReview daysRecalls (K-match)
K921525HIP JOINT METAL/POLYMER SEMI-CONSTRAINED PROTHESISImplant Technology, Inc.1995-01-1110130
K915617LSF HA COATED FEMORAL HIPImplant Technology, Inc.1992-05-281640
K920021LSF TOTAL HIP SYSTEM - MULLER-TYPE ACETABULAR CUPImplant Technology, Inc.1992-03-25830
K913616LSF DIAGNOSTIC RELATED GROUP CEMENTED HIPImplant Technology, Inc.1991-11-07860
K902727LSF CEMENTED FEMORAL HIPImplant Technology, Inc.1990-08-09490
K901460LSF(TM) TOTAL HIP SYSTEMImplant Technology, Inc.1990-05-22550
K891472IMPLANT TECHNOLOGY BONE CEMENT EXTRACTORImplant Technology, Inc.1989-05-02480
K884432MODIFIED LSF TOTAL HIP SYSTEMImplant Technology, Inc.1988-12-09490
K883212LSF (R) TOTAL HIP SYSTEM - BIPOLAR COMPONENTImplant Technology, Inc.1988-11-221160
K855017LSF* TOTAL HIP SYSTEMImplant Technology, Inc.1986-06-111770
K841546COMMUNI-TRACH TUBEImplant Technology, Inc.1984-04-30140
K831511TRACHEOSTOMY TUBEImplant Technology, Inc.1983-07-07560
K823291COMMUNITRACH TUBEImplant Technology, Inc.1983-01-08640

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