Spider Screw Slp-1508
by Hdc Corp.
Spider Screw Slp-1508 is a Class II device made by Hdc Corp., cleared under FDA 510(k) K071851 on 18 Oct 2007 and listed in FDA GUDID since 24 Aug 2016 (UDI-DI 08057013140652), active as of 23 Oct 2026.
Active
510(k)
Valid until
No expiry
FDA recalls
None found
Documents
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number08057013140652 | Date24 Aug 2016 | StatusListed |
| United States | FDA 510(k)SESE | NumberK071851 | Date18 Oct 2007 | StatusActive |
Official records
- AccessGUDID record 08057013140652
- FDA 510(k) database K071851
Across registries
- FDA 510(k) K071851 decided 18 Oct 2007 Active
- FDA GUDID UDI-DI 08057013140652 listed 24 Aug 2016 Listed
Timeline
- Cleared FDA 510(k) K071851
- Listed FDA GUDID 08057013140652
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Spider Screw
- Generic name
- Orthodontic anchoring screw
- Model / Ref / Catalog
- SLP-1508
- Primary DI / UDI-DI
- 08057013140652
- 510(k) Number
- FDA product code
- DZE
- GMDN term
- Orthodontic anchoring screw
- Device class
- Class II
- Regulation number
- 872.3640
- GUDID distribution status
- In Commercial Distribution
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