Atlas FDA

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

Conair Corp. — Predicate Candidate Screening

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

383 daysmedian FDA review time
580 days90th percentile
29clearances measured
K-numberDeviceApplicantDecidedReview daysRecalls (K-match)
K950441CONAIR FAMILY FITNESS BODY ENERGYConair Corp.1995-07-181720
K950410CONAIR BODY AND SOLEConair Corp.1995-05-231120
K944637FAMILY FITNESS SHIATSU MASSAGERConair Corp.1994-12-13830
K943730SQUEEZE PLAYConair Corp.1994-11-281180
K924970FEMININE HEAT WRAPConair Corp.1994-10-037330
K943092FAMILY FITNESS SHIATSU MASSAGERConair Corp.1994-09-29930
K942950BODY FLEXConair Corp.1994-07-26330
K942223BODY SYSTEMConair Corp.1994-06-09340
K940369BODY RECHARGERConair Corp.1994-04-21850
K926339BODY RELAXERConair Corp.1994-03-044440
K911727INFRADERM; TOUCH 'N TONE PLUSConair Corp.1994-02-2510450
K925820ARTHRITIC HEAT WRAPConair Corp.1994-02-024420
K923238SONASSAGEConair Corp.1994-02-025800
K924581HEALTH ESSENTIALS MAXI MASSAGERConair Corp.1993-10-123970
K924582HEALTH ESSENTIALS BODY CARE MASSAGERConair Corp.1993-10-123970
K924584HEALTH ESSENTIALS FANCY PERSONAL MASSAGERConair Corp.1993-10-123970
K924800MOSIST HEAT PAD WITH AUTOMATIC OFFConair Corp.1993-10-123830
K924518BODY SOOTHERConair Corp.1993-10-124030
K924519BODYTHERMConair Corp.1993-10-124030
K924583HEALTH ESSENTIALS MULTI-PURPOSE MASSAGERConair Corp.1993-10-123970
K924431HEALTLH ESSENTIALS PERSONAL MASSAGERConair Corp.1993-10-124060
K924799MOIST HEAT PADConair Corp.1993-10-123830
K924885KING SIZE HEAT PADConair Corp.1993-10-123790
K924520BODY TRAINERConair Corp.1993-09-303910
K915241SPORTS HEAT WRAPConair Corp.1991-12-20370
K915242TOUCH N TONE 1 MASSAGERConair Corp.1991-12-20370
K914344MULTI-REACH II WAND MASSAGERConair Corp.1991-10-24270
K912383VIBRATOUCH II CORDLESS WAND MASSAGERConair Corp.1991-10-071360
K902895INFRASSAGE MASSAGERConair Corp.1990-07-25220

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