PROTEMP H
FDA 510(k) clearance K002364 · decided 2000-08-10
Clearance details
- K-number
- K002364
- Device name
- PROTEMP H
- Applicant
- Espe Dental AG
- Decision
- Substantially Equivalent
- Date received
- 2000-08-03
- Decision date
- 2000-08-10
- Days to decision
- 7 days
- Clearance type
- Special
- Product code
- EBG
- Device class
- 2
- Regulation number
- 872.3770
- Medical specialty
- Dental
- Advisory committee
- Dental
- Location
- Bavaria D-82228 Seefeld, DE
- Third-party review
- No
- Expedited review
- No
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Devices cleared under the same product code - the starting set for predicate research.
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|---|---|---|
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| TEMP MASTER, PMMA-based dental resin (K243951) | Taiwan Dental Materials Co., Ltd. | 2025-02-21 |
| PrimmaArt (K231859) | Dentscare Ltda | 2024-11-26 |
| Digital Temp (K242559) | Sprintray, Inc. | 2024-11-26 |
| Premium Teeth Resin (K240538) | Formlabs Ohio, Inc. | 2024-07-19 |
| Fixtemp® C&B 4:1 (K241226) | Dreve Denatmid GmbH | 2024-05-31 |
| dima Print Teeth & Temp (K233868) | Kulzer, LLC | 2024-05-23 |
| PMMA BLOCK (K223706) | Huliang(Shanghai) Bio-Tech Co., Ltd. | 2023-05-12 |
Recalls involving this device
No recalls on record reference this clearance.