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

Influence, Inc. — Predicate Candidate Screening

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

74 daysmedian FDA review time

90 days90th percentile

16clearances measured

K-number	Device	Applicant	Decided	Review days	Recalls (K-match)
K981677	REPOSE BONE SCREW SYSTEM	Influence, Inc.	1999-08-27	472	2
K991792	CRYO-MONO CRYOGENIC SYSTEM, MODEL CRYO-MONO WITH TUF PROBE	Influence, Inc.	1999-08-12	78	0
K992277	STAPLETAC BONE ANCHOR SYSTEM	Influence, Inc.	1999-07-30	23	0
K991122	CRYO-MONO CRYOGRNIC SYSTEM	Influence, Inc.	1999-07-01	90	0
K990160	MICROTAC-BONE ANCHOR SYSTEM	Influence, Inc.	1999-02-16	28	0
K990095	STRAIGHT-IN-ORTHOPEDIC BONE SCREW FIXATION SYSTEM	Influence, Inc.	1999-02-01	20	0
K983325	IN-PROBE II URODYNAMIC SYSTEM	Influence, Inc.	1998-11-24	63	0
K982155	SHORT STRAIGHT-IN BONE SCREW FIXATION SYSTEM	Influence, Inc.	1998-08-31	74	0
K981631	INFLUENCE CLIP SYSTEM	Influence, Inc.	1998-07-28	82	0
K980482	TRIANGLE SLING	Influence, Inc.	1998-03-27	46	0
K972622	STRAIGHT-IN BONE SCREW FIXATION SYSTEM	Influence, Inc.	1997-10-09	87	0
K972651	IN-SLING	Influence, Inc.	1997-09-19	67	0
K972023	SLEEP-IN BONE SCREW SYSTEM	Influence, Inc.	1997-08-25	84	0
K970292	IN-FAST BONE SCREW SYSTEM/IN-FAST BONE SCREW INSERTER/IN-FAS	Influence, Inc.	1997-04-23	89	1
K964953	IN-TAC BONE ANCHOR SYSTEM	Influence, Inc.	1997-02-13	70	0
K962372	UROTAC BONE ANCHOR INSERTER	Influence, Inc.	1996-08-19	61	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