Facility

MAR-MED 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)	1832653
Establishment type	Manufacture Medical Device
Location	333 Fuller Ave NE Grand Rapids, MI, US 49503
Registration status	Active · expires 2026
Parent company	Mar-Med Inc, (owner-operator 1832653)
Brand names	Derma-Stent

Activity by year

Recalls (1)

Devices registered here (1)

Catheter, Irrigation
Product code GBX (opens in a new tab) · Class I · General, Plastic Surgery · 21 CFR 878.4200

Recalls & enforcement

Class IITerminated2020-12-28
A failure can occur if the user attempts to remove the device by partially snipping the edge and pulling on it. The device may tear into two pieces with a portion remaining in place, which can continue to constrict the vessels. This type of failure can result in digit ischemia.

All facilities operated by Mar-Med 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. “MAR-MED Inc. (FEI 1832653) — FDA facility record.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/facility/1832653-mar-med-inc/

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