Facility

RHONDIUM LIMITED

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)	3011789026
Establishment type	Manufacture Medical Device
Location	4 Sheffield Street Katikati Bay of Plenty, NZ 3129
Registration status	Active · expires 2026
Parent company	RHONDIUM LIMITED (owner-operator 10049515)

Activity by year

Recalls (1)

Devices registered here (1)

Restoration, Resin
Product code NSM (opens in a new tab) · Not classified · Unknown

Recalls & enforcement

Class IICompleted2019-01-31
The product was mislabeled with an incorrect expiration date.

All facilities operated by RHONDIUM LIMITED

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. “RHONDIUM LIMITED (FEI 3011789026) — FDA facility record.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/facility/3011789026-rhondium-limited/

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