Facility

ORTHO ORGANIZERS, 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)	2081322
Establishment type	Repack or Relabel Medical Device; Manufacture Medical Device
Location	800 King George Blvd, Suite 100 Savannah, GA, US 31419
Registration status	Active · expires 2026
Parent company	ORTHO ORGANIZERS , INC. (owner-operator 2081322)
Brand names	Orthoflex Composite Brackets; OrthoFlex Composite Buttons; Composite Direct Bond Button; OrthoFlex Composite Eyelet; Bite-Builder

Activity by year

Recalls (1)

Devices registered here (1)

Bracket, Plastic, Orthodontic
Product code DYW (opens in a new tab) · Class II · Dental · 21 CFR 872.5470

Recalls & enforcement

Class IITerminated2019-04-02
Orthodontic Bracket is mislabeled

All facilities operated by ORTHO ORGANIZERS , 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. “ORTHO ORGANIZERS, INC. (FEI 2081322) — FDA facility record.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/facility/2081322-ortho-organizers-inc/

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