Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR, NMPA) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

Corplex P/ Theracor P/ Allacor P

K-Number: K242828 · 2024-10-18

ApplicantStimlabs, LLC
Decision Date2024-10-18
Product CodeKGN
DecisionSubstantially Equivalent

Device Summary

Corplex P/ Theracor P/ Allacor P is a medical device manufactured by Stimlabs, LLC. It received FDA 510(k) clearance on 2024-10-18 under approval number K242828. The device is classified under product code KGN. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Corplex P/ Theracor P/ Allacor P?

Corplex P/ Theracor P/ Allacor P is a medical device that received FDA 510(k) clearance on 2024-10-18. It is manufactured by Stimlabs, LLC. The 510(k) number is K242828.

When was Corplex P/ Theracor P/ Allacor P approved by the FDA?

Corplex P/ Theracor P/ Allacor P received FDA 510(k) clearance on 2024-10-18, under approval number K242828.

What company makes Corplex P/ Theracor P/ Allacor P?

Corplex P/ Theracor P/ Allacor P is manufactured by Stimlabs, LLC.

What is the FDA product code for Corplex P/ Theracor P/ Allacor P?

The FDA product code for Corplex P/ Theracor P/ Allacor P is KGN.

Other Devices by Stimlabs, LLC

K231325Corplex P / Theracor P / Allacor P K253339Theracor

Related Devices (Code: KGN)

K160136Flowable Wound MatrixCook Biotech Incorporated K152600Collagen Dental Wound DressingsCollagen Matrix, Inc. K153754MicroMatrixAcell, Inc. K153690PriMatrix Dermal Repair ScaffoldTei Biosciences, Inc. K172010gel-e BandageGel-E, Inc. (Formerly Remedium Technologies, Inc.) K171842Geistlich Wound MatrixGeistlich Pharma AG

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

↑