Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under 2 spellings of its name, each linked to the record.
As of Nov 14, 2026, FDA's public records list Procedure Products, Inc. with 16 510(k) clearances and 1 device recall. The most recent is a 510(k) clearance dated Mar 27, 2017: Freedom Syringe.
Drug approvals, 510(k) clearances, recalls and letters, 2017 to 2026 to date
A hatched bar is a year that is not over, so its count covers only part of the year.
| Mar 27, 2017 | Freedom SyringeK161812 · FMF | 510(k) clearances |
| Oct 27, 2015 | U-SDN 2 Part Ultra Modified Seldinger Needles, NS/37-0387. All needles were sold in bulk, non-sterile, and intended for further processinClass II · The firm had received a complaint alleging that a medical professional had difficulty inserting a guide wire into a need | Device recalls |
| Oct 8, 1993 | INSUFFLATOR CONNECTING FILTERK923194 · HIF | 510(k) clearances |
| Dec 10, 1992 | TORQUE DEVICEK922536 · DQX | 510(k) clearances |
| Nov 27, 1991 | CONNECTING SETK914128 · DQO | 510(k) clearances |
| Apr 24, 1991 | BAG SPIGOTK910673 · KPE | 510(k) clearances |
| Dec 20, 1988 | MODIFIED 10CC SYRINGE CONTROL RING SETK884985 · FMF | 510(k) clearances |
| Feb 4, 1988 | 10CC SYRINGE CONTROL RING SETK874747 · FMF | 510(k) clearances |
| Jan 29, 1988 | ANGIO WASTE FLUIDS DUMP BAGK874037 · DQO | 510(k) clearances |
Spellings are joined only when they reduce to the same name, or a reviewed source names the same company. Sharing an FDA establishment number (FEI) is not enough: contract sites make products for many firms. Facts marked AI were labelled by a language model from the firm's FDA names; everything else comes from FDA or Wikidata. How this page is built
