Facility

IMPLANT RESOURCE, 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)	1000139815
Establishment type	Repack or Relabel Medical Device
Location	917 Lone Oak Rd, Suite 1000 Eagan, MN, US 55121
Registration status	Active · expires 2026
Parent company	IMPLANT RESOURCE, INC dba MEDICAL PRODUCTS RESOURCE (owner-operator 9010087)
Brand names	MPR389.265

Activity by year

Recalls (1)

Devices registered here (1)

Orthopedic Manual Surgical Instrument
Product code LXH (opens in a new tab) · Class I · Orthopedic · 21 CFR 888.4540

Recalls & enforcement

Class IIOngoing2021-07-21
Potential for mallet head to become separated from mallet handle. There is also significant deformations on striking surface that were not expected

All facilities operated by IMPLANT RESOURCE, INC dba MEDICAL PRODUCTS RESOURCE

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. “IMPLANT RESOURCE, INC. (FEI 1000139815) — FDA facility record.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/facility/1000139815-implant-resource-inc/

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