ClearanceBrief
Company · IT

Copan Wasp Srl

FDA 510(k) clearances and medical device recalls filed under this name, 2021 to 2026. Name variants (Inc, Corp, punctuation) are merged.

5510(k) clearances (1 in 12 months)
2recalls (1 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
LONSystem, Test, Automated, Antimicrobial Susceptibility, Short Incubation2
QQVAutomated System For Sample Preparation And Identification Of Microorganisms From Cultured Isolates By Mass Spectrometry2
JQPCalculator/Data Processing Module, For Clinical Use1
KZBAutomated Colony Counter1
PPUMicrobial Colony Image Assessment System1

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Jan 22, 2026K251511PhenoMATRIX
Copan Wasp Srl, IT
PPU
Dec 27, 2023K232756Colibrí
Copan Wasp Srl, IT
LON
Mar 20, 2023K223245Colibrí
Copan Wasp Srl, IT
QQV
Oct 5, 2022K220546Colibrí System
Copan Wasp Srl, IT
LON
Dec 27, 2021K193138Colibri System
Copan Wasp Srl, IT
QQV

Latest recalls

DateFirm and productCodeLinked 510(k)
Jul 31, 2026Copan WASP
Brand Name: WASPLab Product Name: WASPLab Model/Catalog Number: W087 Software Version: WebApp version 2.33.1, 2.33.3 and 2.34.2 Product Description: WASPLab is an automated device intended to be used
Open, Classified
JQPNone listed
May 21, 2025Copan WASP
PhenoMATRIX
Open, Classified
KZBNone listed
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