Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under its name, each linked to the record.
As of Nov 13, 2026, FDA's public records list TH Charters, Inc. with 8 510(k) clearances. The most recent is a 510(k) clearance dated Oct 26, 1987: ELECTROBLOC TRANS. ELECTRICAL NERVE BLOCK GENERA..
| Date | Record | Source |
|---|---|---|
| Oct 26, 1987 | ELECTROBLOC TRANS. ELECTRICAL NERVE BLOCK GENERA.K873357 · GZJ | 510(k) clearances |
| May 8, 1986 | EXER-STIM 2K861501 · GZJ | 510(k) clearances |
| Jul 19, 1985 | REMOTE SPEED CONTROLK851946 · ISD | 510(k) clearances |
| Jul 19, 1985 | TORQUE FEEDBACK METERK851967 · ISD | 510(k) clearances |
| Jan 3, 1984 | MINI-1 TRANSCUTANEOUS ELEC-NERVE STIMK834215 · GZJ | 510(k) clearances |
| Jul 19, 1983 | NEURO-PULSER 2 TRANSCUTAN. ELEC. NERVEK831850 · GZJ | 510(k) clearances |
| Oct 6, 1982 | EXER-STIM CONTROLLERK822056 · IPF | 510(k) clearances |
| Mar 19, 1980 | STIM-EX 201K800486 · IPF | 510(k) clearances |
Spellings are joined only when they reduce to the same name, or a reviewed source names the same company. Sharing an FDA establishment number (FEI) is not enough: contract sites make products for many firms. Facts marked AI were labelled by a language model from the firm's FDA names; everything else comes from FDA or Wikidata. How this page is built
