Product code EJP— Dental

FDA has cleared 11 devices under product code EJP between 1980 and 1994, filed by 10 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.

• 19941 clearance
• 19892 clearances
• 19881 clearance
• 19871 clearance
• 19862 clearances
• 19831 clearance
• 19812 clearances
• 19801 clearance

• Almore Intl., Inc.2 clearances
• Williams Gold Refining Co., Inc.1 clearance
• Texapol Corp.1 clearance
• Shofu Dental Corp.1 clearance
• Sds Dental, Inc.1 clearance
• Premier Medical1 clearance
• Ivoclar North America, Inc.1 clearance
• Dentsply Intl.1 clearance
• Bauer, Cheng & Associates, Inc.1 clearance
• Alrand, Inc.1 clearance

• K926190 — ALRAND INC. (DENTAL HAND INSTRUMENTS)Alrand, Inc.·1994-01-18
• K896131 — GNATHOMAT ARTICULATORIvoclar North America, Inc.·1989-12-04
• K892373 — DENTAL PLASTIC BITE FORKTexapol Corp.·1989-06-12
• K884418 — PREMIER DIE-TRAK ARTICULATORPremier Medical·1988-11-14
• K872943 — DISPOSABLE ARTICULATORDentsply Intl.·1987-08-11
• K863009 — GNATUS ARTICULATOR 4.300/4.300GP 8.600 & ORTOFLEXSds Dental, Inc.·1986-09-25
• K854702 — PLASTIC MOUNTING RINGSAlmore Intl., Inc.·1986-03-06
• K833039 — HANDY IIMShofu Dental Corp.·1983-10-04
• K811075 — BALANCE ARTICULATORAlmore Intl., Inc.·1981-05-13
• K810971 — THE GNATOMETBauer, Cheng & Associates, Inc.·1981-05-05
• K801342 — DISPOSABLE ARTICULATORWilliams Gold Refining Co., Inc.·1980-07-08