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

Anchor Products Co. — Predicate Candidate Screening

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

85 daysmedian FDA review time

102 days90th percentile

7clearances measured

K-number	Device	Applicant	Decided	Review days	Recalls (K-match)
K091930	ANCHOR LAPAROSCOPIC TISSUE RETRIEVAL SYSTEM, MODEL TRS100SB	Anchor Products Co.	2009-09-23	85	0
K061555	ANCHOR LAPARSCOPIC TISSUE RETIEVAL SYSTEM	Anchor Products Co.	2006-08-31	87	2
K982073	ANCHOR LAPAROSCOPIC TISSUE RETRIEVAL SYSTEM	Anchor Products Co.	1998-09-22	102	0
K884862	ANCHOR DOUBLE-EDGE MYRINGOTOMY BLADE	Anchor Products Co.	1988-12-27	36	0
K873124	ANCHOR BIOPSY NEEDLE	Anchor Products Co.	1987-09-08	29	0
K831648	ANCHOR BRAND SURGICAL NEEDLES	Anchor Products Co.	1983-08-16	85	0
K790405	ANCHOR BRAND COUNT-TAINER	Anchor Products Co.	1979-03-26	28	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