Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in GermanyLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under its name, each linked to the record.
As of Nov 14, 2026, FDA's public records list Gimmi with 7 510(k) clearances. The most recent is a 510(k) clearance dated Jul 22, 2026: AlphaTriPart - Monopolar MIC Instruments.
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.
| Jul 22, 2026 | AlphaTriPart - Monopolar MIC InstrumentsK261179 · GEI | 510(k) clearances |
| Feb 12, 2010 | ALPHAHYSTEROSCOPE, FIBEROPTIC, OPERATIVE AND DIAGNOSTICK092421 · HIH | 510(k) clearances |
| Jan 27, 2010 | ALPHAXENON LIGHT 180 W AND 300 WK093125 · GCT | 510(k) clearances |
| May 6, 2009 | GIMMI ANEURYSM CLIPS AND APPLYING FORCEPSK081640 · HCH | 510(k) clearances |
| Mar 11, 2002 | GIMMI ALPHA HYSTEROSCOPES & ACCESSORIES, MODELS E.8XXX.XX, T.8XXX.XX, ZXXX.XX,S.XXXX.XX, K0142.25K012869 · HIH | 510(k) clearances |
| Dec 20, 2001 | GIMMI'ALPHA' ENDOSCOPES & ACCESSORIESK012660 · FET | 510(k) clearances |
| Nov 27, 2001 | GIMMI ALPHA SINUSCOPES MODEL # E.8282.01/31/71 + E.8284.01/31/71; GIMMI ALPHA BRONCHOSCOPES MODEL # E.8189.00/01/02/03K013731 · EOQ | 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
