Atlas FDA

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

Litton Dental Products — Predicate Candidate Screening

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

10 daysmedian FDA review time
59 days90th percentile
12clearances measured
K-numberDeviceApplicantDecidedReview daysRecalls (K-match)
K791704MASTERSCALE IILitton Dental Products1979-10-26590
K791024ULTRASONIC DENTAL PROPHYLAXIS UNITLitton Dental Products1979-09-171100
K781114ULTRAMATE 990Litton Dental Products1978-08-14420
K781044ULTRASONIC DENTAL PROPHYLAXIS UNIT,SSMLitton Dental Products1978-06-3080
K772244ILLUMINATED DENTAL HANDPIECELitton Dental Products1978-01-20420
K771556EXRLitton Dental Products1977-08-22100
K771557ULTRASON 990Litton Dental Products1977-08-1970
K771252CB600, TURBINE CONTROL BOLLitton Dental Products1977-07-1540
K771251HU:500, HYGIENASSISTLitton Dental Products1977-07-1540
K761247LT:200, LOVING TOUCHLitton Dental Products1976-12-1630
K761246SONUS IIILitton Dental Products1976-12-1630
K760331TURBINE, AIR DRIVEN HANDPIECE (2000)Litton Dental Products1976-08-11140

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