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Regenerative Biologics, Inc.

FDA Regulatory Profile

Regenerative Biologics, Inc. has 0 FDA recalls, 44 inspections, 0 510(k) clearances and 1 compliance action on record.

Latest inspection
Jul 14, 2026 · NAI

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Summary

Record counts and when each FDA source was last refreshed
RecordsCountLast refreshedSource as ofStatus
Recalls0Nov 4, 2026 (checked Nov 8, 2026, unchanged)File dated Nov 3, 2026Current
510(k) clearances0Nov 8, 2026File dated Nov 2, 2026Current
Inspections44Nov 9, 2026Newest record Oct 28, 2026Current
Compliance actions1Nov 2, 2026Newest record Oct 29, 2026Current

Recent FDA Inspections

DateSiteProductClassificationFEI
Jul 14, 2026Melbourne, FLBiologicsNo Action Indicated (NAI)3003567044
Apr 24, 2026Birmingham, ALBiologicsNo Action Indicated (NAI)3013545785
Nov 18, 2025Alachua, FLBiologicsNo Action Indicated (NAI)1000307669
Nov 5, 2024Gainesville, FLBiologicsNo Action Indicated (NAI)3003567004
Mar 11, 2024Panama City, FLBiologicsNo Action Indicated (NAI)3003567034
Nov 16, 2023Greenville, SCBiologicsNo Action Indicated (NAI)3026137435
Apr 13, 2023Alachua, FLBiologicsNo Action Indicated (NAI)1000307669
Jan 11, 2023Miami, FLBiologicsNo Action Indicated (NAI)3017195536
Aug 1, 2022Fort Myers, FLBiologicsNo Action Indicated (NAI)3014740535
Jul 14, 2022Bradenton, FLBiologicsNo Action Indicated (NAI)3014055282
Sep 15, 2021Brooklyn, NYBiologicsNo Action Indicated (NAI)3016710347
Feb 6, 2020Alachua, FLBiologicsVoluntary Action Indicated (VAI)1000307669
Jul 12, 2019Palm City, FLBiologicsNo Action Indicated (NAI)3012044453
Jun 18, 2019Gainesville, FLBiologicsNo Action Indicated (NAI)3003567004
Mar 28, 2019Pensacola, FLBiologicsNo Action Indicated (NAI)3003567016
Sep 19, 2018Bradenton, FLBiologicsNo Action Indicated (NAI)3014055282
Apr 27, 2018Birmingham, ALBiologicsNo Action Indicated (NAI)3013545785
Dec 6, 2017Fresno, CABiologicsNo Action Indicated (NAI)3030733598
Nov 27, 2017Margate, FLBiologicsNo Action Indicated (NAI)3013532046
Aug 15, 2017Alachua, FLBiologicsNo Action Indicated (NAI)1000307669

NAI means no objectionable conditions or practices were found during the inspection. VAI means objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action. OAI means regulatory and/or administrative actions are recommended.

FDA-Inspected Facilities

FacilityLocationInspectionsLatest
FEI 3003567044Melbourne, FL4Jul 14, 2026
FEI 3013545785Birmingham, AL2Apr 24, 2026
FEI 1000307669Alachua, FL7Nov 18, 2025
FEI 3003567004Gainesville, FL6Nov 5, 2024
FEI 3003567034Panama City, FL2Mar 11, 2024
FEI 3026137435Greenville, SC1Nov 16, 2023
FEI 3017195536Miami, FL1Jan 11, 2023
FEI 3014740535Fort Myers, FL1Aug 1, 2022
FEI 3014055282Bradenton, FL2Jul 14, 2022
FEI 3016710347Brooklyn, NY1Sep 15, 2021
FEI 3012044453Palm City, FL2Jul 12, 2019
FEI 3003567016Pensacola, FL3Mar 28, 2019
FEI 3030733598Fresno, CA1Dec 6, 2017
FEI 3013532046Margate, FL1Nov 27, 2017
FEI 3003567064Tallahassee, FL4Jun 14, 2017
FEI 3003567027Jacksonville, FL3May 16, 2017
FEI 3009510408Tampa, FL2Sep 30, 2014
FEI 3010949999Lake Worth, FL1Sep 12, 2014

FDA data resources

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