Facility

OBP Medical Corporation

1 recall(s) on record — most severe on record: Class II.

Key facts

1recalls · worst Class II

1inspections · worst VAI

—warning letters in our data

Recalls are listed for the parent company: openFDA recall records do not name a facility. How we attribute records

FDA Establishment Identifier (FEI)	3007789561
Establishment type	Develop Specifications But Do Not Manufacture At This Facility
Location	360 MERRIMACK STREET Lawrence, MA, US 01843
Registration status	Active · expires 2026
Parent company	OBP Medical Corporation (owner-operator 10025921)
Brand names	SURE-SCOPE

Activity by year

Recalls (1)
Inspections (1)

Devices registered here (1)

Laryngoscope, Rigid
Product code CCW (opens in a new tab) · Class I · Anesthesiology · 21 CFR 868.5540

Recalls & enforcement

Class IIOngoing2026-07-13
There is a potential for vaginal speculums to contain a burr on the proximal plastic blade, which may introduce a sharp edge in the contact regions for both the patient and the healthcare provider.

FDA inspections (1)

VAI2016-12-09
Voluntary Action Indicated · Compliance: Devices · citations posted

Source: U.S. FDA Inspections Dashboard (opens in a new tab) (device inspection classifications, 2016–present). Data as of 2026-10-06. The dashboard profile can take several seconds to load.

All facilities operated by OBP Medical Corporation

Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this facility record at FDA → (opens in a new tab)

Cite this record

RegWarden. “OBP Medical Corporation (FEI 3007789561) — FDA facility record.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/facility/3007789561-obp-medical-corporation/

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