Spiggle & Theis Medizintechnik
Medical device makerAI in GermanyAI. FDA records under its name, each linked to the record.
- Records across the group: 2, 2 entitiesAI
- 510(k) clearances: 1
- Device recalls: 1
Records by Year
Drug approvals, 510(k) clearances, recalls and letters, 2017 to 2026 to date, Spiggle & Theis Medizintechnik and its 1 subsidiaries
Latest Records
Newest first across sources; each opens the record| Date | Record | Source |
|---|---|---|
| Jun 27, 2025 | Injection needle, bayonet, Luer-Lock, 1. Model no. 50-353-23, working length 25 cm, total length 31cm, nonsterile; 2. Model no. 50-345Class II · Affected product show elevated cytotoxicity values. Use of affected injection needles may present a risk of intolerance | Device recalls |
| Aug 3, 2023 | TubaVent Balloon Dilatation SystemK223542 · PNZ | 510(k) clearances |
Subsidiaries and Divisions
1 firms in the Spiggle & Theis Medizintechnik group, most records first- Spiggle & Theis Mt Gmbh1 records
Canada and Imports
Across the Spiggle & Theis Medizintechnik group, matched by company name- Active Health Canada device licences
- 15, as of Nov 10, 2026
Names and Identifiers
- Appears as
- Website
- spiggle-theis.de
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