Facility

Cadence Inc.

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

Key facts

2recalls · worst Class II

1inspections · worst NAI

—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)	3009266751
Establishment type	Manufacture Medical Device for Another Party (Contract Manufacturer)
Location	9 Technology Dr Staunton, VA, US 24401
Registration status	Active · expires 2026
Parent company	Cadence, Inc. (owner-operator 2414164)

Activity by year

Recalls (2)
Inspections (1)

Devices registered here (1)

Orthopedic Manual Surgical Instrument
Product code LXH (opens in a new tab) · Class I · Orthopedic · 21 CFR 888.4540

Recalls & enforcement

Class IITerminated2019-05-10
The glass syringe used with Pressure Control Syringes may potentially break during use.
Class IITerminated2015-07-09
Graduation marks of the syringe are not centered with the numeric position marks on the syringe barrel.

FDA inspections (1)

NAI2017-12-14
No Action Indicated · Compliance: Devices; Postmarket Assurance: Devices

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.

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. “Cadence Inc. (FEI 3009266751) — FDA facility record.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/facility/3009266751-cadence-inc/

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