Facility

MYOFUNCTIONAL RESEARCH CO. USA

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)	3005505603
Establishment type	Repack or Relabel Medical Device
Location	9267 Charles Smith Ave Rancho Cucamonga, CA, US 91730
Registration status	Active · expires 2026
Parent company	MYOFUNCTIONAL RESEARCH CO USA INC (owner-operator 9002061)
Brand names	Lingual Tubes BWS

Activity by year

Recalls (1)

Devices registered here (1)

Tube, Orthodontic
Product code DZD (opens in a new tab) · Class I · Dental · 21 CFR 872.5410

Recalls & enforcement

Class IIOngoing2025-10-09
Due to firm mistakenly distributing product within the U.S. without FDA premarket clearance/approval.

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. “MYOFUNCTIONAL RESEARCH CO. USA (FEI 3005505603) — FDA facility record.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/facility/3005505603-myofunctional-research-co-usa/

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