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

Smith & Nephew Perry — Predicate Candidate Screening

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

189 daysmedian FDA review time

244 days90th percentile

10clearances measured

K-number	Device	Applicant	Decided	Review days
K932665	ENCORE POWDER-FREE SURGICAL GLOVES MICROPTIC	Smith & Nephew Perry	1993-12-22	203
K932664	ENCORE POWDER-FREE SURGICAL GLOVES ORTHOPAEDIA	Smith & Nephew Perry	1993-12-22	203
K931399	PERRY ENHANCED PROTECTION LATEX SURGICAL GLOVE	Smith & Nephew Perry	1993-11-18	244
K923929	PERRY POWDER-FREE GLOVES, STYLE 45G	Smith & Nephew Perry	1993-02-10	189
K922379	STERILE LATEX EXAMINATION GLOVES	Smith & Nephew Perry	1992-09-22	125
K914445	PERRY(R) NATURAL POWDER-FREE GLOVES, STYLE 45	Smith & Nephew Perry	1992-04-22	201
K914942	PERRY(R) CUT-RESISTANT GLOVES	Smith & Nephew Perry	1992-01-31	88
K913402	PERRY(R) DERMAGUARD(R) PLUS GLOVES	Smith & Nephew Perry	1991-10-02	64
K911633	PERRY(R) ENCORE CHEMOTHERAPY GLOVE	Smith & Nephew Perry	1991-05-09	28
K905537	PERRY XTENDA CUFF SURGICAL GLOVES	Smith & Nephew Perry	1991-01-11	31

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