Sscor, Inc.
United StatesFDA applicant, unverified FDA FEI 2022724
Sscor, Inc. is a medical device manufacturer, with 39 devices listed in FDA GUDID and FDA 510(k) (FDA Class II) and 6 FDA recalls as of 14 Nov 2026.
- Devices
- 39
- Registrations
- FDA
- FDA recalls
- 6
Registry facts
- Registries
- FDA GUDID 34
- FDA 510(k) 5
- Device classes
- FDA Class II 39
- FDA recalls
- Identifiers
- FDA FEI 2022724
- DUNS 131254971
At a glance
Market reach
- United States
- FDA FEI, FDA recalls
Catalogue
Search and filter all 39 devicesCompany details
- FDA FEI number
- 2022724
- DUNS number
- 131254971
- Address
- 2125 N. Madera Rd Unit C, Simi Valley, CA, 93065
FDA recalls
2005
- 6 Jan 2005 Z-0411-05 Unclassified (pre-2012) 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.
- 6 Jan 2005 Z-0412-05 Unclassified (pre-2012) 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.
- 6 Jan 2005 Z-0413-05 Unclassified (pre-2012) 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.
- 6 Jan 2005 Z-0414-05 Unclassified (pre-2012) 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.
- 6 Jan 2005 Z-0415-05 Unclassified (pre-2012) 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.
- 6 Jan 2005 Z-0416-05 Unclassified (pre-2012) 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.
Frequently asked questions
How many devices does SSCOR, INC. have in the registry?
The registry currently lists 39 devices for SSCOR, INC.. Devices recorded under merged duplicate company entries are counted once.
Which registries list SSCOR, INC.'s devices?
Among its 39 most recently registered devices, SSCOR, INC. has devices listed in FDA 510(k) (5 devices) and FDA GUDID (34 devices). A device can be listed in more than one registry, so these counts overlap.
What risk classes do SSCOR, INC.'s devices fall under?
Among its 39 most recently registered devices, the classes recorded for SSCOR, INC.'s devices are Class II. Each device page shows its own class and authorisation.
Are there FDA recall records for SSCOR, INC.?
FDA recall records list 6 recalls initiated by SSCOR, INC., the most recent initiated on 6 Jan 2005. A recall is often a precaution started by the manufacturer; the records say nothing about the company's overall record.
What are the newest devices from SSCOR, INC. in the registry?
The most recently registered devices listed for SSCOR, INC. include SSCOR DCell H DM10-001H, S-SCORT® TEN 2100, S-SCORT® II 15006 and SSCOR QUICKDRAW® 2403.