Miscellaneous devices · 21 CFR 872 Subpart G
Endodontic Dry Heat Sterilizer
Call for PMAs on 4/21/97 per 62 FR 2902 on 1/21/97
- Companies listing it
- 00 makers
- Brands and models
- 0
- 510(k) clearances
- 00 in five years
- FDA name
- Sterilizer, Endodontic Dry Heat
Official records: FDA product classification for KOK · 21 CFR 872.6730.
Source: FDA establishment registration & device listing, 510(k) and product classification files · FDA data as of 2 Nov 2026 · snapshot 12 Nov 2026