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

EGG — Predicate Candidate Screening

24 FDA 510(k) clearances under this product code; the 50 most recent screened below.

69 daysmedian FDA review time

164 days90th percentile

24clearances measured

K-number	Device	Applicant	Decided	Review days
K990979	STECO-TITANMAGNETICS	Steco-System-Technik GmbH & Cokg	1999-09-03	164
K950259	COUPLING DEVICE FOR DENTAL PROSTHESIS	Dr. Joseph E. Grasso, D.D.S.	1996-12-06	683
K925700	ZEST ANCHOR ADVANCED GENERATION	Zest Anchors, Inc.	1994-04-07	511
K915299	COGAN CORP KITS OF DENTAL HAND INSTRUMENTS	Cogan Corp.	1992-01-31	73
K912435	DENTAL CONNECTOR PRECISION ATTACHMENT	Metalor Dental USA Corp.	1991-08-28	86
K912567	CONICAST, INTRACAST, OMECAST	Metalor Dental USA Corp.	1991-07-02	21
K901928	INTERPORE IMZ(CASTABLE)TUB/SCRET RET RIGID ATTACH	Interpore Intl.	1990-07-26	90
K900785	MICRO 2 SYSTEM	Inodent	1990-04-16	55
K896337	DENTAL BRIDGE ANCHORING PINS	Gayso Bridge-Tech, Inc.	1990-01-31	89
K895986	PRECISION DENTAL ATTACHMENTS	Implant Support Systems, Inc.	1989-10-18	90
K891119	T.R.S.: TOOTH REPLACEMENT SYSTEM	Health Technology of America, Inc.	1989-04-17	46
K882063	MAGNE-DENT MAGNET/ZEST RETROFIT KEEPER	Zest Anchors, Inc.	1988-06-13	28
K871439	COSMETIC SINGLE SPAN BRIDGE	Cosmetic Dental Technologies, Inc.	1987-06-08	56
K870331	IMZ INTRAMOBILE CYLINDER IMPLANT SYSTEM COMPONENTS	Interpore Intl.	1987-03-02	33
K863243	SHINER STRESS DIRECTING ATTACHMENT	Js & R - R & D Co.	1986-10-30	69
K861561	ZEST MARK II (STANDARD & MINI)	Zest Anchors, Inc.	1986-05-21	26
K855167	DYNA SYSTEM	Parker Laboratories, Inc.	1986-03-04	68
K854633	JACKSON RARE EARTH MAGNETIC ATTACHMENT	Solid State Innovations, Inc.	1986-01-30	72
K840600	MAGNE-DENT	Magne-Dent	1984-04-30	80
K830439	DENTA A-33	Denta, Inc.	1983-05-09	88
K823280	DISTAFLEX	Duradent Corp.	1982-11-22	19
K812360	PRECIOUS-METAL/PLASTIC ATTACH., AUXILL	Zl-Microdent-Attachments	1981-09-21	32
K791788	MICRO-RING SYSTEM PRECISION ATTACH.	Howmedica Corp.	1979-10-22	41
K780711	MICRO-RING	Howmedica Corp.	1978-05-26	29

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