Consumer health companyLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in United StatesLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field., part of Procter & GambleLabelled by claude-sonnet-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under its name, each linked to the record.
As of Nov 15, 2026, FDA's public records list Procter & Gamble Manufacturing Co. with 72 510(k) clearances. The most recent is a 510(k) clearance dated Jan 19, 1988: SCENTED OR SCENTED DEODORIZED MENSTRUAL PADS.
| Jan 19, 1988 | SCENTED OR SCENTED DEODORIZED MENSTRUAL PADSK873457 · HIL | 510(k) clearances |
| Jan 19, 1988 | ATTENDS INCONTINENT BRIEFK873036 · EYQ | 510(k) clearances |
| Jan 21, 1987 | UNSCENTED MENSTRUAL PADK864673 · HHL | 510(k) clearances |
| Aug 11, 1986 | MODIFIED PROTECTIVE GARMENTK861863 · EYQ | 510(k) clearances |
| Jul 2, 1986 | SINGLE-USE PATIENT UNDERPADK862348 · KME | 510(k) clearances |
| Mar 5, 1986 | MODIFIED PROTECTIVE GARMENT FOR INCONTINENTSK860598 · EYQ | 510(k) clearances |
| Oct 16, 1985 | ATTENDS DISPOS. UNDERPADK853880 · KME | 510(k) clearances |
| Sep 6, 1985 | SCENTED ALWAYS PANTILINERSK853000 · HHL | 510(k) clearances |
Spellings are joined only when they reduce to the same name, or a reviewed source names the same company. Sharing an FDA establishment number (FEI) is not enough: contract sites make products for many firms. Facts marked AI were labelled by a language model from the firm's FDA names; everything else comes from FDA or Wikidata. How this page is built
