Facility

RyMed Technologies, LLC

1 recall(s) on record — most severe on record: Class II.

Key facts

1recalls · worst Class II

2inspections · worst VAI

—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)	3005951712
Establishment type	Develop Specifications But Do Not Manufacture At This Facility
Location	6000 W. William Cannon Drive Austin, TX, US 78749
Registration status	Active · expires 2026
Parent company	RyMed Technologies, LLC (owner-operator 10045258)
Brand names	InVision-Plus® with Neutral Advantage? technology IV Connector; InVision-Plus® RED? with Neutral Advantage? technology IV Connector; InVision-Plus® Junior® with Neutral Advantage? technology IV Connector

Activity by year

Recalls (1)
Inspections (2)

Devices registered here (1)

Set, Administration, Intravascular
Product code FPA (opens in a new tab) · Class II · General Hospital · 21 CFR 880.5440

Recalls & enforcement

Class IITerminated2016-01-05
Potential for the female luer component of the InVision-Plus IV connector to crack during use.

FDA inspections (2)

NAI2025-08-28
No Action Indicated · Compliance: Devices; Postmarket Assurance: Devices
NAI2022-06-24
No Action Indicated · Compliance: Devices; Postmarket Assurance: Devices · citations posted

Source: U.S. FDA Inspections Dashboard (opens in a new tab) (device inspection classifications, 2016–present). Data as of 2026-10-06. The dashboard profile can take several seconds to load.

All facilities operated by RyMed Technologies, LLC

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. “RyMed Technologies, LLC (FEI 3005951712) — FDA facility record.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/facility/3005951712-rymed-technologies-llc/

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