Atlas FDA

Predicate Research Report · generated 2026-08-21 · Print / save as PDF · Save to account

Hoveround Corp. — Predicate Candidate Screening

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

63 daysmedian FDA review time
279 days90th percentile
17clearances measured
K-numberDeviceApplicantDecidedReview daysRecalls (K-match)
K122741HOVEROUND TEKNIQUEHoveround Corp.2013-05-072420
K122707HOVERROUND TEKNIQUEHoveround Corp.2013-05-072450
K100527HOVEROUND TEKNIQUE, MODEL HD-6Hoveround Corp.2010-03-26300
K093946HOVEROUND HOVERGLIDE MODEL HOVERGLIDE MK-2Hoveround Corp.2010-03-22890
K100350HOVEROUND TEKNIQUE GT POWER WHEELCHAIR, MODEL# TEKNIQUE GTHoveround Corp.2010-03-22380
K090108HOVEROUND TEKNIQUE FWD MK4 POWER WHEELCHAIRHoveround Corp.2009-03-19630
K043069HOVEROUND E100 POWER CHAIRHoveround Corp.2004-12-03250
K042920HOVEROUND SE-3 POWERCHAIRHoveround Corp.2004-12-03421
K042545HOVEROUND MPV-5 POWERCHAIRHoveround Corp.2004-10-21310
K042033HOVEROUND POWER WHEELCHAIR, MODEL HD700Hoveround Corp.2004-09-29620
K022993HOVEROUND REHAB SEATING SYSTEM FOR POWER WHEELCHAIRSHoveround Corp.2002-12-02840
K021136TEKNIQUE-HOVEROUND POWER WHEEL CHAIRHoveround Corp.2002-04-19100
K010075TEKNIQUEHoveround Corp.2001-02-14360
K991132ACTIVAHoveround Corp.1999-10-202010
K954131HOVEROUND POWER WHEELCHAIR OR HVR-200 BY HOVEROUNDHoveround Corp.1996-06-062790
K935410HOVEROUND MPVHoveround Corp.1994-03-281390
K932329HOVEROUND POWER CHAIRHoveround Corp.1994-03-283190

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