Facility

VITREQ BV

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)	3012037425
Establishment type	Manufacture Medical Device
Location	Seggelant-Noord 2 Vierpolders Zuid-Holland, NL 3237 MG
Registration status	Active · expires 2026
Parent company	VITREQ BV (owner-operator 10050448)
Brand names	Depressor, orbital

Activity by year

Recalls (1)

Devices registered here (1)

Depressor, Orbital
Product code HNX (opens in a new tab) · Class I · Ophthalmic · 21 CFR 886.4350

Recalls & enforcement

Class IITerminated2019-12-17
Microscopic tears of the sterile pouch may compromise sterility

All facilities operated by VITREQ BV

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. “VITREQ BV (FEI 3012037425) — FDA facility record.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/facility/3012037425-vitreq-bv/

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