Cardiva Medical, Inc. FDA Record

Warning letters, Form 483s, inspections, recalls and 510(k) clearances

Cardiva Medical, Inc. has 0 FDA recalls, 9 inspections, 7 510(k) clearances and 0 compliance actions on record. No FDA warning letter addressed to "Cardiva Medical, Inc." is on file.

What these totals cover: FDA records filed under the name "Cardiva Medical, Inc." and its spelling variant "Cardiva Medical".

Latest inspection
Jul 21, 2023 · VAI
Latest 510(k)
Mar 14, 2013

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Summary

Record counts and when each FDA source was last refreshed
RecordsCountLast refreshedSource as ofStatus
Recalls0Nov 8, 2026File dated Nov 3, 2026Current
510(k) clearances7Nov 8, 2026File dated Nov 2, 2026Current
Inspections9Nov 14, 2026Newest record Nov 5, 2026Current
Compliance actions0Nov 2, 2026Newest record Oct 29, 2026Current

FDA record by year

Cardiva Medical, Inc.'s FDA inspections, warning letters and recalls in each of the last 10 calendar years (2017 to 2026, 2026 so far).

Cardiva Medical, Inc.: FDA inspections per year 2017: 1 inspections120172018: 0 inspections020182019: 1 inspections120192020: 0 inspections020202021: 0 inspections020212022: 0 inspections020222023: 1 inspections120232024: 0 inspections020242025: 0 inspections020252026: 0 inspections02026
YearInspectionsOAIWarning lettersRecall recordsClass I
202600000
202500000
202400000
202310000
202200000
202100000
202000000
201910000
201800000
201710000

Inspections are counted by the date they ended, warning letters by the date FDA issued them and recall records by the recall start date. FDA lists one recall record per recalled product, so one recall event can add several.

Recent FDA inspections

9 inspections from Sep 3, 2009 to Jul 21, 2023.

DateSiteProductClassificationFEI
Jul 21, 2023Santa Clara, CADevicesVoluntary Action Indicated (VAI)3015145497
Mar 14, 2019Santa Clara, CADevicesNo Action Indicated (NAI)3015145497
May 10, 2017Santa Clara, CADevicesVoluntary Action Indicated (VAI)3015145497
Dec 15, 2016Guaymas, MexicoDevicesNo Action Indicated (NAI)3011469355
Mar 25, 2014Santa Clara, CADevicesNo Action Indicated (NAI)3015145497
Nov 19, 2012Santa Clara, CADevicesVoluntary Action Indicated (VAI)3015145497
Oct 30, 2012Santa Clara, CADevicesNo Action Indicated (NAI)3015145497
May 4, 2012Santa Clara, CADevicesNo Action Indicated (NAI)3015145497
Sep 3, 2009Santa Clara, CADevicesVoluntary Action Indicated (VAI)3015145497
NAI
No objectionable conditions or practices were found during the inspection.
VAI
Objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action.
OAI
Regulatory and/or administrative actions are recommended.

Look up the inspector observations behind these results with the FDA 483 search, or check for formal enforcement with the FDA warning letter search.

FDA-inspected facilities

2 inspected sites, newest inspection first.

FacilityLocationInspectionsLatest
FEI 3015145497Santa Clara, CA8Jul 21, 2023
FEI 3011469355Guaymas, Mexico1Dec 15, 2016

Recent 510(k) clearances

7 510(k) clearances from Oct 22, 2004 to Mar 14, 2013.

K-NumberDeviceDate
K130124CATALYST II AND IIIMar 14, 2013
K082930CARDIVA CATALYST III SYSTEM WITH PROTAMINE SULFATEFeb 13, 2009
K072297BOOMERANG CATALYST/BOOMERANG CATALYST II SYSTEMSep 12, 2007
K070485BOOMERANG WIRE /BOOMERANG PLUS WIRE SYSTEM, MODEL# B PLUS WIRE 58LMar 22, 2007
K051817BOOMERANG CLOSUREWIRE VASCULAR CLOSURE SYSTEMDec 6, 2006
K061075BOOMERANG WIRESep 1, 2006
K041486VASOSTASIS VASCULAR CLOSURE SYSTEMOct 22, 2004

Cardiva Medical, Inc. and the FDA: common questions

Has Cardiva Medical, Inc. received an FDA warning letter?

No FDA warning letter addressed to the name "Cardiva Medical, Inc." is on file. This answer covers that name only: letters addressed to a related company name or to one of its sites are listed on that name's or site's own page.

Has Cardiva Medical, Inc. received an FDA Form 483?

FDA has not published a Form 483 for "Cardiva Medical, Inc." in its reading room. FDA publishes some Form 483s, not all of them.

When did the FDA last inspect Cardiva Medical, Inc.?

The most recent FDA inspection on file ended Jul 21, 2023 at Santa Clara, CA and was classified VAI. FDA has 9 inspections of Cardiva Medical, Inc. on file.

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Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.