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Sign in to claim this brandSpiggle & Theis Medizintechnik GmbH
US
Last updated September 17, 2026
What Spiggle & Theis Medizintechnik GmbH makes
Spiggle & Theis Medizintechnik GmbH manufactures reusable surgical instruments for soft-tissue manipulation, including alligator forceps, irrigation/aspiration cannulas, and retraction tools. Their portfolio also includes specialized ENT devices such as nasal scissors, suction dissectors, and ear speculums, alongside precision instruments like micro forceps and suture hooks. Additional products include reusable curettes for endaural procedures and reusable tubular forceps for controlled tissue handling.
The company’s devices are classified under FDA’s Class I and Class II categories and are listed in the FDA’s Unique Device Identifier (UDI) database. Their instruments are designed for reusable medical use in surgical and otolaryngology applications, adhering to regulatory standards for reusable surgical tools in the United States.
Written from this company's registered devices by an AI model, and not verified by a human reviewer.
Frequently asked questions
What does Spiggle & Theis Medizintechnik GmbH manufacture?
Spiggle & Theis Medizintechnik GmbH manufactures reusable surgical instruments for soft-tissue manipulation, including alligator forceps, irrigation/aspiration cannulas, and retraction tools. They also produce specialized ENT devices such as nasal scissors, suction dissectors, and ear speculums, alongside precision instruments like micro forceps and suture hooks.
Where is Spiggle & Theis Medizintechnik GmbH based?
Spiggle & Theis Medizintechnik GmbH is based in the United States, as indicated by the country designation 'US' in the provided device data.
Which regulatory registries list Spiggle & Theis Medizintechnik GmbH's devices?
Spiggle & Theis Medizintechnik GmbH's devices are listed in the FDA's Unique Device Identifier (UDI) database, as specified in the device data.
How are Spiggle & Theis Medizintechnik GmbH's devices classified?
Spiggle & Theis Medizintechnik GmbH's devices are classified under FDA's Class I and Class II categories, as indicated in the device data. These classifications reflect the level of control necessary to ensure the safety and effectiveness of the devices.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- US
- Address
- —
- Website
- spiggle-theis.com
- —
- —
- [email protected]
- Phone
- +492206908165
- PRRC Contact
- —
- EUDAMED SRN
- —
- FDA FEI Number
- —
- DUNS Number
- 332893028
Catalogue (2840)
Page 57 of 57| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Scalpel blades | 10-360-10 | FDA UDI | Class I | Active |
| Heymann nasal scissors | 20-683-18 | FDA UDI | Class I | Active |
| Ear forceps | 15-609-85 | FDA UDI | Class I | Active |
| Volkmann retractor | 80-330-04 | FDA UDI | Class I | Active |
| Jeweler forceps | 10-507-11 | FDA UDI | Class I | Active |
| DeBakey vascular forceps | 15-487-15 | FDA UDI | Class I | Active |
| Brünings tip | 40-579-00 | FDA UDI | Class I | Active |
| Farabeuf retractor | 85-313-15 | FDA UDI | Class I | Active |
| Dandy artery forceps | 40-650-01 | FDA UDI | Class I | Active |
| Micro ear forceps, comfort | 10-703-13 | FDA UDI | Class I | Active |
| Dingmann teeth hooks, movable | 40-327-99 | FDA UDI | Class I | Active |
| Antrum punch | 30-300-03 | FDA UDI | Class I | Active |
| T-tube inserter, dismountable | 10-760-00 | FDA UDI | Class I | Active |
| Septal splints | 72-3035 BT | FDA UDI | Class I | Active |
| Sterile equipment drape | 2500140H | FDA UDI | Class II | Active |
| Cottle osteotome | 20-408-04 | FDA UDI | Class I | Active |
| Langenbeck raspatory | 10-348-19 | FDA UDI | Class I | Active |
| ENT-single-use suction tubes, angled | 303025U | FDA UDI | Class II | Active |
| Bipolar connecting cable | 80-319-50 | FDA UDI | Class II | Active |
| Perkins retractor | 10-433-11 | FDA UDI | Class I | Active |
| Spoon curette, semi-sharp | 90-201-19 | FDA UDI | Class I | Active |
| Bipolar Forceps | 80-201-01 | FDA UDI | Class II | Active |
| Scissors, Premium Line | 20-648-12 | FDA UDI | Class I | Active |
| Kocher artery forceps | 80-370-14 | FDA UDI | Class I | Active |
| Wullstein micro hook | 10-628-06 | FDA UDI | Class I | Active |
| Stevens vascular scissors Black Line | 20-623-11WB | FDA UDI | Class I | Active |
| Frazier suction tube | 30-080-09 | FDA UDI | Class I | Active |
| Bipolar connecting cable | 80-328-30 | FDA UDI | Class II | Active |
| Rochester-Pean artery forceps | 80-383-22 | FDA UDI | Class I | Active |
| Metzenbaum-Fino scissors | 20-607-20 | FDA UDI | Class I | Active |
| Draf ethmoid forceps | 30-724-13 | FDA UDI | Class I | Active |
| ENT-single-use suction tubes, angled | 303020 | FDA UDI | Class II | Active |
| Metzenbaum scissors Black Line | 20-615-15WB | FDA UDI | Class I | Active |
| Spoon curette | 90-212-02 | FDA UDI | Class I | Active |
| Total Middle Ear Implant | 11600 | FDA UDI | Class II | Active |
| Buck ear curette | 10-261-20 | FDA UDI | Class I | Active |
| Rubin osteotome | 20-412-03 | FDA UDI | Class I | Active |
| Draf ethmoid forceps | 30-722-16 | FDA UDI | Class I | Active |
| Beckmann adenoid curette | 40-201-02 | FDA UDI | Class I | Active |
| Mirror, round, 5 mm, polished | 90-222-05 | FDA UDI | Class I | Active |
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