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SSCOR, INC.

Last updated September 17, 2026

Information

Country: US
Address: 2125 N. Madera Rd Unit C, Simi Valley, CA, 93065
Website: —
LinkedIn: —
Facebook: —
Email: —
Phone: —
PRRC Contact: —
EUDAMED SRN: —
FDA FEI Number: 2022724
DUNS Number: 131254971

Catalogue (38)

Device	Model / Reference	Registries	Class	Status
S-Scort® Ten	2100	FDA UDI	Class II	Unknown
S-Scort® Ii	15006	FDA UDI	Class II	Unknown
Sscor Quickdraw®	2403	FDA UDI	Class II	Active
SSCOR/board	23001-WCK	FDA UDI	Class II	Active
Sscor Quickdraw®	2402	FDA UDI	Class II	Unknown
SSCOR/board	22500	FDA UDI	Class II	Active
Sscor Quickdraw®	2403OD	FDA UDI	Class II	Active
Sscor Quickdraw®	2401	FDA UDI	Class II	Unknown
Sscor Quickdraw®	2400	FDA UDI	Class II	Unknown
S-SCORT® lll	74000	FDA UDI	Class II	Active
SSCOR/board	22000-PLC	FDA UDI	Class II	Active
SSCOR/board	23001-WC	FDA UDI	Class II	Active
SSCOR/board	23001	FDA UDI	Class II	Active
SSCOR/board	23001-WCKK	FDA UDI	Class II	Active
S-Scort® 9	2109	FDA UDI	Class II	Unknown
S-Scort® Ten	2100S	FDA UDI	Class II	Unknown
Sscor Vx-2 ®	2310V-230	FDA UDI	Class II	Active
SSCOR/board	22020-LDR	FDA UDI	Class II	Active
SSCOR/board	23001-PLC	FDA UDI	Class II	Active
SSCOR/board	22000-GIFA	FDA UDI	Class II	Active
SSCOR DCell	DM10-001	FDA UDI	Class II	Active
SSCOR/board	23001B	FDA UDI	Class II	Active
Sscor Vx-2®	2310V	FDA UDI	Class II	Active
SSCOR Duet ®	2314BV-230	FDA UDI	Class II	Active
SSCOR/board	25000	FDA UDI	Class II	Active
SSCOR Duet ®	2314NB	FDA UDI	Class II	Active
Sscor Duet	2314	FDA UDI	Class II	Active
SSCOR/board	22000	FDA UDI	Class II	Active
Sscor Duet	2314B	FDA UDI	Class II	Active
SSCOR/board	22000-BRAUN	FDA UDI	Class II	Active
SSCOR/board	22000-RRC	FDA UDI	Class II	Active
Sscor Vx-2 ®	2310BV-230	FDA UDI	Class II	Active
Sscor Vx-2®	2310BV	FDA UDI	Class II	Active
S-Scort(r)duet Model 2014 Portable Suction Pump	K945929	FDA 510(k)	Class II	Active
S-Scort...jr Quickdraw, Model 2400	K041154	FDA 510(k)	Class II	Active
S-Scort	K952632	FDA 510(k)	Class II	Active
S-Scort (2500)	K964997	FDA 510(k)	Class II	Active
Sscor/Board ..3 Model 23000 Pre-Assembled Suction System For Patient Transport Vehicles	K950464	FDA 510(k)	Class II	Active

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FDA Recalls (6)

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
Jan 6, 2005	Z-0413-05	—	terminated	Reports from medical professionals that SSCOR suction device has not performed as intended. Firm's investigation disclosed that the condition in questions is caused by cracked regulators that result in inadequate suction.
Jan 6, 2005	Z-0415-05	—	terminated	Reports from medical professionals that SSCOR suction device has not performed as intended. Firm's investigation disclosed that the condition in questions is caused by cracked regulators that result in inadequate suction.
Jan 6, 2005	Z-0412-05	—	terminated	Reports from medical professionals that SSCOR suction device has not performed as intended. Firm's investigation disclosed that the condition in questions is caused by cracked regulators that result in inadequate suction.
Jan 6, 2005	Z-0411-05	—	terminated	Reports from medical professionals that SSCOR suction device has not performed as intended. Firm's investigation disclosed that the condition in questions is caused by cracked regulators that result in inadequate suction.
Jan 6, 2005	Z-0416-05	—	terminated	Reports from medical professionals that SSCOR suction device has not performed as intended. Firm's investigation disclosed that the condition in questions is caused by cracked regulators that result in inadequate suction.
Jan 6, 2005	Z-0414-05	—	terminated	Reports from medical professionals that SSCOR suction device has not performed as intended. Firm's investigation disclosed that the condition in questions is caused by cracked regulators that result in inadequate suction.