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

Procter & Gamble Co. — Predicate Candidate Screening

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

64 daysmedian FDA review time

223 days90th percentile

23clearances measured

K-number	Device	Applicant	Decided	Review days	Recalls (K-match)
K141018	ORAL-B TEST DRIVE POWER BRUSH TRIAL PROGRAM KIT, ORAL-B TEST	Procter & Gamble Co.	2014-09-15	147	0
K131543	TAMPAX(R) L PLASTIC TAMPONS, UNSCENTED	Procter & Gamble Co.	2013-06-20	22	0
K091281	TAMPAX PEARL UNSCENTED TAMPONS, LIGHT, REGULAR, SUPER & SUPE	Procter & Gamble Co.	2010-06-01	396	0
K091964	CREST GLIDE CLINICAL GUM PROTECTION DENTAL FLOSS	Procter & Gamble Co.	2009-09-24	85	0
K081555	TAMPAX PEARL PLASTIC APPLICATOR TAMPONS, SCENTED AND UNSCENT	Procter & Gamble Co.	2008-06-27	24	1
K062638	TAMPAX COMPAK PEARL PLASTIC APPLICATOR SCENTED AND UNSCENTED	Procter & Gamble Co.	2006-11-22	78	0
K061486	TAMPAX TAMPONS - (LIGHT,REGULAR,SUPER AND SUPER PLUS ABSORBE	Procter & Gamble Co.	2006-08-01	62	0
K051290	TAMPAX PEARL PLASTIC APPLICATOR TAMPONS, ULTRA ABSORBENCY (U	Procter & Gamble Co.	2005-12-27	223	0
K040999	TAMPAX TAMPONS (JUNIOR, REGULAR, SUPER AND SUPER PLUS ABSORB	Procter & Gamble Co.	2004-07-09	81	0
K040312	TAMPAX PEARL SCENTED TAMPONS-JUNIOR, REGULAR, SUPER & SUPER	Procter & Gamble Co.	2004-05-03	84	0
K012629	ALWAYS DUETS	Procter & Gamble Co.	2001-10-05	53	0
K011996	TAMPAX PEARL SCENTED AND UNSCENTED TAMPONS - JUNIOR, REGULAR	Procter & Gamble Co.	2001-09-19	84	0
K011171	TAMPAX SCENTED & SATIN SCENTED TAMPAX-JUNIOR, REGULAR, SUPER	Procter & Gamble Co.	2001-07-02	76	0
K003843	ENVIVE MINIFORMS	Procter & Gamble Co.	2001-02-08	58	0
K002096	TAMPAX SATIN TAMPONS, CLOSED END FLUSHABLE APPLICATOR; TAMPA	Procter & Gamble Co.	2000-09-08	59	0
K993870	UNSCENTED INTERLABIAL MENSTRUAL PAD	Procter & Gamble Co.	2000-01-18	64	0
K973236	CREST TOOTHBRUSH WITH MICROSHIELD	Procter & Gamble Co.	1998-03-11	195	0
K945200	FIXODENT, FIXODENT FRESH, FASTEETH AND EXTRA HOLD FASTEETH D	Procter & Gamble Co.	1994-11-30	36	2
K922575	ALWAYS CONTOURS UNSCENTED MENSTRUAL PADS	Procter & Gamble Co.	1993-02-02	246	0
K913238	ALWAYS, UNSCENTED MENSTRUAL PAD	Procter & Gamble Co.	1991-09-23	63	0
K913237	ALWAYS, SCENTED/SCENTED DEODORIZED MENSTRUAL PAD	Procter & Gamble Co.	1991-09-23	63	0
K884428	ALWAYS UNSCENTED MENSTRUAL PADS	Procter & Gamble Co.	1988-12-02	43	0
K884429	ALWAYS SCENTED OR SCENTED DEODORIZED MENSTRUAL PAD	Procter & Gamble Co.	1988-12-02	43	0

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