Atlas FDA

Predicate Research Report · generated 2026-08-23 · Print / save as PDF · Save to account

Bruno Independent Living Aids, Inc. · Predicate Candidate Screening

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

28 daysmedian FDA review time
145 days90th percentile
12clearances measured
K-numberDeviceApplicantDecidedReview daysRecalls (K-match)
K113308BRUNO ELAN STAIRWAY ELEVATORBruno Independent Living Aids, Inc.2012-02-01840
K061514BRUNO VERTICAL PLATFORM LIFT, MODEL VPL-3100Bruno Independent Living Aids, Inc.2006-07-13420
K033829BRUNO ELECTRA-RIDE III STAIRWAY ELEVATOR SYSTEM, MODEL CRE-2Bruno Independent Living Aids, Inc.2003-12-29200
K033752BRUNO ELECTRA-RIDE STAIRWAY ELEVATOR SYSTEM. MODEL SRE-1540Bruno Independent Living Aids, Inc.2003-12-12110
K033438BRUNO ELECTRA-RIDE ELITE, MODEL SRE-2000Bruno Independent Living Aids, Inc.2003-11-20230
K022509BRUNO ELECTRA-RIDE, MODEL SRE-2700Bruno Independent Living Aids, Inc.2002-08-13140
K011227REGAL MOTOTRIZED 3 WHEELED VEHICLEBruno Independent Living Aids, Inc.2001-05-11180
K002205CARONYBruno Independent Living Aids, Inc.2000-08-10200
K991954THE BRUNO POWERBASE, MODEL PSB-2200Bruno Independent Living Aids, Inc.1999-11-021450
K970927BRUNO ELECTRA-RIDE III STAIRWAY ELEVATOR SYSTEMBruno Independent Living Aids, Inc.1997-08-261660
K921647REGAL MOTORIZIED 3 WHEELED VEHICLEBruno Independent Living Aids, Inc.1992-05-04280
K921648BRUNO ELECTRA-RIDE STAIR-WAY ELEVATOR SYSTEMBruno Independent Living Aids, Inc.1992-05-04280

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