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

Teca, Inc. — Predicate Candidate Screening

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

83 daysmedian FDA review time

212 days90th percentile

29clearances measured

K-number	Device	Applicant	Decided	Review days
K962283	EEG ELECTRODES	Teca, Inc.	1996-12-16	186
K903731	SAPPHIRE SERIES 1P, 1L, 2L, AND 2ME	Teca, Inc.	1991-02-04	172
K903004	EE1114, 1118, 1121 ELECTRO-ENCEPHALOGRAPH	Teca, Inc.	1990-11-15	129
K896666	P460, DG32 ELECTROENCEPHALOGRAPH	Teca, Inc.	1990-02-16	81
K894889	TECA NEUROMAPPER 386	Teca, Inc.	1989-12-22	143
K894088	TECA NEUROMAPPER 1620, BRAIN MAPPER	Teca, Inc.	1989-11-15	160
K890881	TECA 1A96, 1A97 AND 1A98 ELECTROENCEPHALOGRAPHS	Teca, Inc.	1989-03-23	30
K884870	TECA/MEDELEC 'CONCEPT' P420	Teca, Inc.	1989-02-23	94
K880593	TECA/MEDELEC MISTRAL	Teca, Inc.	1988-04-06	55
K872931	TECA/MEDELEC TTT THERMAL THRESHOLD TESTER	Teca, Inc.	1987-11-16	112
K862906	TECA/MEDELEC AS-10 SENSOR	Teca, Inc.	1987-02-04	188
K863156	TECA/MEDELEC AUDIOSTAR	Teca, Inc.	1987-02-03	169
K861069	TECA NEUROPTO WITH OS-5 STIMULATOR	Teca, Inc.	1987-01-27	313
K863749	TECA/ECEM T5 PORTABLE ELECTROENCEPHALOGRAPH	Teca, Inc.	1986-10-06	12
K850137	TECA TC2-64 TRANSCRANIAL DOPPLER	Teca, Inc.	1985-08-14	212
K851232	TECA MONTAGE II	Teca, Inc.	1985-06-13	79
K844481	NEUROLAB II	Teca, Inc.	1985-05-20	182
K850071	TECA MF-20 MICROVASCULAR DOPPLER	Teca, Inc.	1985-04-02	83
K842886	TECA MS-20 MYSTRO ELECTROPHYSIOLOGICAL	Teca, Inc.	1984-12-12	142
K834442	LED STIMULATOR LS-05	Teca, Inc.	1984-08-08	236
K822744	#ST10 PROGR. EVOKED RESPONSE STIMULATOR	Teca, Inc.	1982-11-03	54
K820908	TECA MODEL SENSOR ER 94	Teca, Inc.	1982-05-03	32
K813009	TECA VISUAL/AUDIO STIMULATOR MODEL CS-2	Teca, Inc.	1981-12-14	48
K812715	TECA #TE 8	Teca, Inc.	1981-10-13	18
K802637	TECA MODEL-10 ELECTROMYOGRAPH	Teca, Inc.	1980-11-26	35
K781399	TECA MODEL B9 ELECTROMYOGRAPH	Teca, Inc.	1978-09-20	36
K781398	TECA VS6 VIDEO STIMULATOR	Teca, Inc.	1978-08-23	8
K771188	REVERSING CLICK GENERATOR RCG6	Teca, Inc.	1977-07-14	13
K761220	TECA MODEL SP5/T ELECTRO-THER. STIM.	Teca, Inc.	1976-12-17	10

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