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COOK VANDERGRIFT INC.

United States·US-MF-000002657

Last updated September 17, 2026

Information

Page 2 of 2

Device	Model / Reference	Registries	Class	Status
Byrd	G26514	FDA UDI	Class I	Active
Cook Flexipet	G46021	FDA UDI	Class II	Active
Byrd	G20525	FDA UDI	Class I	Active
Sof-Grip Hemostat	G20001	FDA UDI	Class I	Active
Evolution	G49652	FDA UDI	Class II	Active
Byrd	G20000	FDA UDI	Class I	Active
Byrd	G20535	FDA UDI	Class I	Active
Micro-Injection Pipette	K-MPIP-3135	EUDAMEDFDA UDI	Class IIa	Active
Micro-Injection Pipette	K-MPIP-1035	EUDAMEDFDA UDI	Class IIa	Active
Holding Pipette	K-HPIP-3335	EUDAMEDFDA UDI	Class I	Active
Holding Pipette	K-HPIP-2130	EUDAMEDFDA UDI	Class I	Active
Blastomere Aspiration Pipette	K-EBPH-3035	EUDAMEDFDA UDI	Class IIa	Active
Pin Vise Polymer	LR-PVP001	EUDAMEDFDA UDI	Class I	Active
Doppler Blood Flow Monitor Channel/Cable Verifier	DP-MCV01	EUDAMEDFDA UDI	Class I	Active
Holding Pipette	K-HPIP-1030	EUDAMEDFDA UDI	Class I	Active
Holding Pipette	K-HPIP-2135	EUDAMEDFDA UDI	Class I	Active
Micro-Injection Pipette	K-MPIP-3330	EUDAMEDFDA UDI	Class IIa	Active
Micro-Injection Pipette	K-MPIP-3135	EUDAMEDFDA UDI	Class IIa	Active
Micro-Injection Pipette	K-MPIP-1030	EUDAMEDFDA UDI	Class IIa	Active
Blastomere Aspiration Pipette	K-EBPH-3535	EUDAMEDFDA UDI	Class IIa	Active
Micro-Injection Pipette	K-MPIP-1020	EUDAMEDFDA UDI	Class IIa	Active
Charger for Doppler Blood Flow Monitor	DP-M350-CHG1	EUDAMEDFDA UDI	Class I	Active
Holding Pipette	K-HPIP-1035	EUDAMEDFDA UDI	Class I	Active
Holding Pipette	K-HPIP-3330	EUDAMEDFDA UDI	Class I	Active
Micro-Injection Pipette	K-MPIP-3130	EUDAMEDFDA UDI	Class IIa	Active

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Not available yet.

Recalls reported by this firm to the FDA. Listed at company level — FDA recall records don't identify a specific catalogue device.

Date	Recall No.	Class	Status	Reason
Jul 24, 2023	Z-2513-2023	—	open, classified	Sterility of device may be compromised due to breach of the chevron seal of the packaging