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

Medical Products Development, Inc. — Predicate Candidate Screening

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

38 daysmedian FDA review time

108 days90th percentile

13clearances measured

K-number	Device	Applicant	Decided	Review days
K810013	MULTIPERFECTEMP CAUTERY	Medical Products Development, Inc.	1981-04-23	108
K810016	REPLACABLE BATTERY PERFECTEMP CAUTERY	Medical Products Development, Inc.	1981-04-23	108
K810012	MULTIMICRO SURGICAL CAUTERY	Medical Products Development, Inc.	1981-04-23	108
K803067	SURG-FLEX 10 LIGHT	Medical Products Development, Inc.	1981-02-26	84
K810015	MULTIHI-TEMP CAUTERY	Medical Products Development, Inc.	1981-02-12	38
K810014	REPLACABLE BATTERY HI-TEMP CAUTERY	Medical Products Development, Inc.	1981-02-12	38
K802942	HITEMP. TM 2 LOOPTIP CAUTERY	Medical Products Development, Inc.	1981-02-04	77
K810019	SURG-FLEX 15 SURGICAL LIGHT	Medical Products Development, Inc.	1981-01-23	18
K810018	SURG-FLEX 5 SURGICAL LIGHT	Medical Products Development, Inc.	1981-01-23	18
K810017	MICROSURG CAUTERY	Medical Products Development, Inc.	1981-01-05	0
K802330	HI-TEMP LOOPTIP SURGICAL CAUTERY	Medical Products Development, Inc.	1980-11-12	50
K801323	HI-TEMP SURGICAL CAUTERY	Medical Products Development, Inc.	1980-06-26	20
K801078	PERFECTEMP OPHTHALMIC CAUTERY	Medical Products Development, Inc.	1980-06-04	28

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