Atlas FDA

Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account

Pacific Dental Corp. — Predicate Candidate Screening

22 FDA 510(k) clearances under this manufacturer; the 50 most recent screened below.

19 daysmedian FDA review time
19 days90th percentile
22clearances measured
K-numberDeviceApplicantDecidedReview daysRecalls (K-match)
K821782BEACH ANESTHETIC SYRINGE CARTR. TYPEPacific Dental Corp.1982-07-20330
K821785BEACH AMALGAM CARVERPacific Dental Corp.1982-07-06190
K821783BEACH SILICATE FILLING & LINING APPLIC.Pacific Dental Corp.1982-07-06190
K821778BEACH DRESSING PLIERPacific Dental Corp.1982-07-06190
K821780BEACH EXPLORER NO. 23T.G.Pacific Dental Corp.1982-07-06190
K821789BEACH CURETTE NO. 2 AND NO. 3 T.G.Pacific Dental Corp.1982-07-06190
K821787BEACH SURGICAL PLIERS NON-HOOKPacific Dental Corp.1982-07-06190
K821788BEACH DERIOSTEAL ELEVATOR, #2 STRAIGHTPacific Dental Corp.1982-07-06190
K821790BEACH EXCAVATOR'S NO. 1 & NO. 2Pacific Dental Corp.1982-07-06190
K821777BEACH MOUTH MIRRORPacific Dental Corp.1982-07-06190
K821784BEACH GINGIVAL RETRACTION INSTR. TYPE BPacific Dental Corp.1982-07-06190
K821779BEACH AMALGAM CARRIER, GUN TYPEPacific Dental Corp.1982-07-06190
K821786BEACH SCALERSPacific Dental Corp.1982-07-06190
K821781BEACH FORCEP NO. 150 AND NO. 151Pacific Dental Corp.1982-07-02150
K821739J. MORITA FLEX M-3 TORX HARDPIECEPacific Dental Corp.1982-06-25110
K801688TORX HANDPIECE CONTRA ANGLES ATTACHMENTSPacific Dental Corp.1980-08-04140
K801687TORX MICRO-MOTOR LOW SPEED HANDPIECEPacific Dental Corp.1980-08-04140
K801682SPACELINE HIGH VOLUME EVACUATION HANDPIEPacific Dental Corp.1980-08-04140
K801685SPACELINE DENTAL CHAIR-UNITPacific Dental Corp.1980-08-04140
K801683LUNA-VUE DENTAL OPERATING LIGHTPacific Dental Corp.1980-08-04140
K801686SPACELINE THREE WAY SYRINGEPacific Dental Corp.1980-08-04140
K801684ASTRON AIR POWERED HIGH SPEED DE PIECEPacific Dental Corp.1980-08-04140

Methodology

Recall counts reflect FDA recall records explicitly referencing each K-number; FDA links recalls to K-numbers inconsistently, so 0 means "none found in FDA records," not "never recalled." Data: FDA openFDA, refreshed weekly. Verify decisions of consequence against the primary source. Full candidate set and CSV export: atlasbyauro.com.

Prepared with Atlas

Predicate research, review-time statistics and recall monitoring for 510(k) teams — atlasbyauro.com/fda