Corbin Clinical Resources, LLC

Cumberland, MD, US

CORBIN CLINICAL RESOURCES, LLC appears in FDA device records in Cumberland, MD. FDA records list 2 510(k) clearances between 2016-08-01 and 2016-09-02, no PMA records and one registered establishment. As of 2026-09-10, FDA records show no recalls for this company, and at least one establishment registration is current.

510(k) clearances: 2
PMA records: 0
Recall records: 0
Registered establishments: 1

510(k) clearance history

FDA records hold 2 510(k) clearances for Corbin Clinical Resources, LLC in 2016.

Clearances by year, as a table

510(k) clearance decisions for Corbin Clinical Resources, LLC, by decision year
Year	Clearances
2016	2

510(k) clearances on record, most recent first
K number	Device	Product code	Decision	Decision date
K160423	Perineologic Access Needle	FCG	Substantially Equivalent	2016-09-02
K160414	Precision Point Biopsy Needle Guide	ITX	Substantially Equivalent	2016-08-01

Registered establishments

FDA registered establishments for Corbin Clinical Resources, LLC, with the product codes listed at each
Registration	FEI	Establishment	Address	Registration expires	Product codes listed
3012975098	3012975098	CORBIN CLINICAL RESOURCES, LLC	183 North Centre Street, Cumberland, MD 21502 US	2026	FCG ITX

Registration numbers link to the FDA registration and listing record for that establishment.

FDA product codes

Recall records

No recall records for this company in the ingested FDA data.

Verification record

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Data as of 2026-09-28, FDA export datePage updated 2026-09-05Source: openFDA, public domain