510(k) Report

FDA applicant

Rymed Technologies, Inc.

Woodward, OK4 decisions1996–20175 recalls

FDA records 4 decisions for Rymed Technologies, Inc. (Woodward, OK) from 1996 to 2017: 4 510(k) clearances. All are in product code FPA (Set, Administration, Intravascular). Its devices cite 6 predicates, 2 of them its own earlier devices. 5 recalls are linked to its devices.

FDA’s records also spell it “Rymed Technologies, LLC”.

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly, last Nov 3, 2026

FIG. A — Illustration, general hospital panel, where it files most

How often FDA has decided Rymed Technologies, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

1in 2017

2010: 12017: 1
2007high 1 (2010) · low 0 (2007)2026

2026 so far, outlined.

Recalls per year

2in 2016

2016: 2
2007high 2 (2016) · low 0 (2007)2026

Class I Class II/III not classified

FIG. 1 — Rymed Technologies, Inc. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Rymed Technologies, Inc.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

See the 510(k) Report

Which product codes does it file in?

  • FPASet, Administration, Intravascular4decisions

Whose devices does it build on?

Its devices cite 6 predicates; 2 are its own earlier devices. The firms it cites most:

Who builds on its devices?

Later devices cite its devices 3 times; 2 of those are its own. The firms that cite it most:

Which of its devices are cited most?

Its devices that later submissions most often claim equivalence to.

  • K991653Invision-Plus Injection Port Connector SystemRymed Technologies, Inc. · 19993cite it

What has FDA decided for it lately?

  • K162826Encore NeutralRymed Technologies, LLC · 2017
  • K093489IN Vision-Plus Nano with Neutral Advantage TechnologyRymed Technologies, Inc. · 20101 recall
  • K991653Invision-Plus Injection Port Connector SystemRymed Technologies, Inc. · 19994 recalls
  • K960771Slav and Slav-One Injection Port Connector SystemRymed Technologies, Inc. · 1996

All 3 as Rymed Technologies, Inc. →The one decision as Rymed Technologies, LLC →

What has been recalled?

5 recalls linked to its devices; the latest:

  • K991653InVision-Plus and InVision-Plus Junior Needleless IV Connector, Disposable, Single Use…Jan 5, 2016Class II
  • K093489InVision-Plus CS Needleless IV Connector, Catalog Number RYM-7001. Disposable, Single…Jan 5, 2016Class II
  • K991653RYM-5000 InVision-Plus Neutral Displacement I.V. Connector, packaged 200 units per box…May 25, 2006
  • K991653RYM-5000 InVision-Plus NEUTRAL I.V. Connector, packaged 200 units per box, 5 boxes per…May 25, 2006
  • K991653RYM-5001 InVision-Plus Neutral Displacement I.V. Connector, packaged 100 units per box…May 25, 2006