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W.H.P.M. INC.

Last updated May 23, 2026

Information

Country: US
Address: —
Website: —
LinkedIn: —
Facebook: —
Email: —
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PRRC Contact: —
EUDAMED SRN: —
FDA FEI Number: —
DUNS Number: 602085672

Catalogue (137)

Page 3 of 3

Device	Model / Reference	Registries	Class	Status
Ecoii	ECOII-87114	FDA UDI	Class II	Active
One-Step	WTC-25	FDA UDI	Class II	Active
ECO™ III Cup	ECOⅢ-254 W/AD	FDA UDI	Class II	Active
ECO™ Cup	WECCUP654	FDA UDI	Class II	Active
ECO™ II Cup	ECOII-4104	FDA UDI	Class II	Active
ECO™ II Cup	ECOII-32104 W/AD	FDA UDI	Class II	Active
ECO™ II Cup	ECOII-13124 W/AD	FDA UDI	U	Active
ECO™ Cup	WECCUP454 W/AD	FDA UDI	Class II	Active
First Sign	W454-FS	FDA UDI	Class II	Unknown
CRL Stat Dip Card	KCUR920121	FDA UDI	U	Active
ECO™ II Cup	ECOII-4574	FDA UDI	U	Active
ECO™ Cup	WECCUP264	FDA UDI	Class II	Active
ECO® II Cup	ECOII-7064	FDA UDI	Class II	Active
ECO™ V Cup	ECOV-264	FDA UDI	Class II	Active
Crl Stat	KCUR920093	FDA UDI	Class II	Active
ECO™ II Cup	ECOII-58104	FDA UDI	U	Active
ECO™ Cup	WECCUP1844	FDA UDI	Class II	Active
ECO™ II Cup	ECOII-254 W/AD6	FDA UDI	Class II	Active
ECO™ Cup	WECCUP2454	FDA UDI	Class II	Active
ECO™ II Cup	ECOⅡ-3104	FDA UDI	Class II	Active
ECO® II Cup	ECOII-7264	FDA UDI	Class II	Active
ECO II Cup ®	ECOII-9124 W/AD6	FDA UDI	Class II	Active
ECO™ II Cup	ECOII-184	FDA UDI	U	Active
ECO™ II Cup	CECOII-874 W/AD4	FDA UDI	Class II	Active
First Sign Drug of Abuse Dip Card Test, First Sign Drug of Abuse Cup Test	K151441	FDA 510(k)	Class II	Active
First Sign Multi-Drug Test Dip Card, First Sign Multi-Drug Test Cup, First Sign Multi-Drug Screen Test Dip Card, First Sign Multi-Drug Screen Test Cup	K210327	FDA 510(k)	Class II	Active
Wh Accu Test One-Step Urine/Serum Combo Pregnancy Test	K051841	FDA 510(k)	Class II	Active
First Sign Drug Of Abuse Screening Test	K032575	FDA 510(k)	Class II	Active
Wh Accu Test Pregnancy Test	K012284	FDA 510(k)	Class II	Active
First Sign Drug Of Abuse Urine Screening Test	K052197	FDA 510(k)	Class II	Active
First Sign Drug of Abuse Dip Card Test (MDMA, EDDP, Nortriptyline), First Sign Drug of Abuse Cup Test (MDMA, EDDP, Nortriptyline)	K160793	FDA 510(k)	Class II	Active
First Sign Drug of Abuse Dip Card Test/First Sign Drug of Abuse Cup Test	K142353	FDA 510(k)	Class II	Active
Hemosure One-Step Fecal Occult Blood Test	K041202	FDA 510(k)	Class II	Active
First Sign Drug of Abuse Dip Card Test, First Sign Drug of Abuse Cup Test	K150162	FDA 510(k)	Class II	Active
First Sign® Drug of Abuse Buprenorphine Cup Test, First Sign® Drug of Abuse Buprenorphine Dip Card Test, First Sign® Drug of Abuse Butalbital Cup Test, First Sign® Drug of Abuse Butalbital Dip Card Test, First Sign® Drug of Abuse Morphine Cup Test, First Sign® Drug of Abuse Morphine Dip Card Test.	K152551	FDA 510(k)	Class II	Active
Hemosure Accu-Reader A100	K200754	FDA 510(k)	Class II	Active
First Sign Multi-Drug Dip Card Test, First Sign Multi-Drug Cup Test, First Sign Drug of Abuse Dip Card Test Marijuana, First Sign Drug of Abuse Cup Test Marijuana	K171695	FDA 510(k)	Class II	Active

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FDA Recalls (1)

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
Mar 4, 2022	Z-0892-2022	—	terminated	Frm became aware that a customer complaint was reported to US FDA that SARS-CoV-2 Antigen Tests were sold domestically by a pharmacy in California. These Antigen Tests have not received FDA Emergency Use Authorization, nor have these tests been cleared or approved by FDA for commercial distribution in the U.S.