Product code EMH— Dental
586 TO 596 VARIOUS TYPES DENTAL ROOT SPLINTER FORC
- Classification name
- Forceps, Rongeur, Surgical
- Device class
- Class 1
- Regulation
- 21 CFR 872.4565
- Advisory panel
- Dental
- Total cleared
- 8
- First cleared
- Most recent
Market context for product code EMH
FDA has cleared devices under product code EMH between 1977 and 1989, filed by 7 applicant companies. No FDA device recalls reference this product code. Class I devices are low-risk and subject to FDA general controls; many Class I device types are exempt from 510(k) premarket notification.
Clearances per year
- 1989
- 1986
- 1985
- 1984
- 1982
- 1977
Top applicants under product code EMH
Recent clearances under product code EMH
- K890255 — BONE RONGEUR, SINGLE-ACTION
- K890256 — BONE RONGEUR, DOUBLE-ACTION
- K854887 — MANU/SURG INST/ACCESS WUERZBURG TIT MINI BONE PLAT
- K851710 — 586 TO 596 VARIOUS TYPES DENTAL ROOT SPLINTER FORC
- K834190 — JAKOBI SURG. INSTRUMENTS #8 15
- K834366 — SURGICAL INSTRUMENTS & ACCESSORIES
- K821358 — MODIFIED RONGEURS FOR SPINAL & ORTH. S.
- K771522 — FORCEPS, STYLE #849
Data sourced from openFDA. This site is unofficial and independent of the FDA.