Facility

OSTEOGENICS BIOMEDICAL, INC.

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

Key facts

1recalls · worst Class II

—inspections in our data

—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)	3002253367
Establishment type	Manufacture Medical Device for Another Party (Contract Manufacturer)
Location	4620 71st St Bldg 78-79 LUBBOCK, TX, US 79424
Registration status	Active · expires 2026
Parent company	OSTEOGENICS BIOMEDICAL, INC. (owner-operator 9028315)
Brand names	Vitala

Activity by year

Recalls (1)

Devices registered here (1)

Barrier, Animal Source, Intraoral
Product code NPL (opens in a new tab) · Class II · Dental · 21 CFR 872.3930

Recalls & enforcement

Class IITerminated2016-09-07
The device has the potential to be packaged in the wrong product box.

All facilities operated by OSTEOGENICS BIOMEDICAL, INC.

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. “OSTEOGENICS BIOMEDICAL, INC. (FEI 3002253367) — FDA facility record.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/facility/3002253367-osteogenics-biomedical-inc/

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