Atlas FDA

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

Dow Corning Corp. Healthcare Industries Materials · Predicate Candidate Screening

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

41 daysmedian FDA review time
171 days90th percentile
31clearances measured
K-numberDeviceApplicantDecidedReview daysRecalls (K-match)
K853186SILASTIC INFLATABLE BONE PLUG H.P.Dow Corning Corp. Healthcare Industries Materials1985-09-24560
K844637WHITESIDE ACRYLIC CEMENT SPACER SLEEVEDow Corning Corp. Healthcare Industries Materials1985-06-192030
K850255DOW CORNING WRIGHT TITANIUM WRIST JOINT GROMMETDow Corning Corp. Healthcare Industries Materials1985-05-01990
K843995TF-II HIP PROSTHESISDow Corning Corp. Healthcare Industries Materials1985-04-231940
K842559WHITESIDE ORTHOLOC TOTAL HIP FEMORALDow Corning Corp. Healthcare Industries Materials1984-12-201710
K840357SSA HIP PROSTHESISDow Corning Corp. Healthcare Industries Materials1984-02-17220
K831479METAL-BACKED ACETABULAR CUPDow Corning Corp. Healthcare Industries Materials1983-06-15370
K812864SILASTIC VOICE PROSTHESISDow Corning Corp. Healthcare Industries Materials1981-11-24420
K812053SILASTIC HEMI WRIST IMPLANT H.P. (RAD.)Dow Corning Corp. Healthcare Industries Materials1981-08-18280
K811679SILASTIC TENDON PASSER H.P.Dow Corning Corp. Healthcare Industries Materials1981-07-10250
K801175SILASTIC II MAMMARY IMPLANTDow Corning Corp. Healthcare Industries Materials1980-12-182160
K801042SILASTIC BRAND PERCUTANEOUS SKIN EXPANDEDow Corning Corp. Healthcare Industries Materials1980-06-26550
K801094SILASTIC HAMMERTOE IMPLANT (SWANSON-WELLDow Corning Corp. Healthcare Industries Materials1980-06-09320
K800898SILASTIC BONE PLUG H.P.(CEMENT RESTRICT)Dow Corning Corp. Healthcare Industries Materials1980-05-02140
K800140SILASTIC SCLERAL SPONGE II W/CIRCLING BDDow Corning Corp. Healthcare Industries Materials1980-03-03420
K800014DOW CORNING/W RIGHT WOUND DRAINAGE SYSDow Corning Corp. Healthcare Industries Materials1980-01-17130
K790914SILASTIC INTRAVENOUS CATHETER UNITDow Corning Corp. Healthcare Industries Materials1979-07-03500
K781870IMPLANT, H.P. CONDYLARDow Corning Corp. Healthcare Industries Materials1979-02-09980
K781664SILASTIC NEPHROSTOMY SYSTEMDow Corning Corp. Healthcare Industries Materials1979-01-221160
K781756SILASTIC H.P. TRAPEXIAL IMPLANTDow Corning Corp. Healthcare Industries Materials1978-11-15300
K781526SILASTIC U-TUBE KITDow Corning Corp. Healthcare Industries Materials1978-09-20150
K780484SILASTIC BRAND PENILE IMPLANTDow Corning Corp. Healthcare Industries Materials1978-07-171120
K780470H.P. MEDICAL GRADE SILICONE TUBINGDow Corning Corp. Healthcare Industries Materials1978-04-27360
K780132IMPLANT, HINGE TOE, FLEX.Dow Corning Corp. Healthcare Industries Materials1978-02-06130
K771548SILASTIC BRAND INTRAVAGINAL TARSETTEDow Corning Corp. Healthcare Industries Materials1977-11-07870
K771558SILASTIC BRAND OBSTETRICAL VACUUM CUPDow Corning Corp. Healthcare Industries Materials1977-09-20360
K760708SILASTIC BRAND Q7-2091 GASTRIC SUMP TUBEDow Corning Corp. Healthcare Industries Materials1976-11-23590
K760860SILASTIC ILEAL RESERVOIR CATHETERDow Corning Corp. Healthcare Industries Materials1976-11-23360
K760943SILASTIC BRAND GASTRIC LAVAGE TUBEDow Corning Corp. Healthcare Industries Materials1976-11-23220
K760945SILASTIC PERCUTANEOUS GASTROINTEST. TUBEDow Corning Corp. Healthcare Industries Materials1976-11-23220
K760700SILASTIC BRAND G7-2090ADow Corning Corp. Healthcare Industries Materials1976-11-02410

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